Dopamine/all

Dopamine synthesis[edit]

DDC

	On chromosome	Chromosome position	In gene	Summary
rs2060762	7	50,461,686	DDC
rs2242041	7	50,461,751	DDC
rs771317809	7	50,470,140	DDC
rs771317809(C;C)	7	50,470,140	DDC	common in clinvar
rs3757472	7	50,470,285	DDC
rs11761683(T;T)	7	50,475,181	DDC	Migraine
rs11761683	7	50,475,181	DDC
rs201951824	7	50,476,625	DDC
rs201951824(C;C)	7	50,476,625	DDC	common in clinvar
rs11575461	7	50,479,485	DDC
rs12718541(A;A)	7	50,482,446	DDC	Nicotine dependence
rs12718541	7	50,482,446	DDC
rs1451371	7	50,485,353	DDC
rs137853209(T;T)	7	50,495,369	DDC	common in clinvar
rs137853209	7	50,495,369	DDC
rs137853212(G;G)	7	50,499,201	DDC	common in clinvar
rs137853212	7	50,499,201	DDC
rs3779084	7	50,501,037	DDC
rs880028	7	50,502,438	DDC
rs137853208(C;C)	7	50,504,025	DDC	common in clinvar
rs137853208	7	50,504,025	DDC
rs6592961	7	50,505,192	DDC
rs7809758	7	50,505,635	DDC
rs1470750	7	50,508,950	DDC
rs3735273	7	50,529,166	DDC
rs137853210	7	50,529,339	DDC
rs137853210(A;A)	7	50,529,339	DDC	common in clinvar
rs998850	7	50,539,690	DDC DDC-AS1
rs137853207	7	50,539,926	DDC DDC-AS1
rs137853207(G;G)	7	50,539,926	DDC DDC-AS1	common in clinvar
rs137853211(C;C)	7	50,539,958	DDC DDC-AS1	common in clinvar
rs137853211	7	50,539,958	DDC DDC-AS1
rs7809234	7	50,542,681	DDC DDC-AS1
rs1085307991	7	50,544,015	DDC
rs1085307991(T;T)	7	50,544,015	DDC	common in clinvar
rs6264	7	50,544,037	DDC
rs6264(G;G)	7	50,544,037	DDC	common in complete genomics
rs2044859(T;T)	7	50,544,864	DDC	Migraine
rs2044859	7	50,544,864	DDC
rs11974297(G;G)	7	50,550,562	DDC	Migraine
rs11974297	7	50,550,562	DDC
rs2329340(T;T)	7	50,552,531	DDC	M
rs2329340	7	50,552,531	DDC
rs1451375	7	50,555,014	DDC
rs921451	7	50,555,587	DDC
rs3837091(AGAG;AGAG)	7	50,561,043	DDC	common in clinvar
rs3837091	7	50,561,043	DDC
rs12540874	7	50,597,225	GRB10

TH

	On chromosome	Chromosome position	In gene	Summary
rs4366464	11	2,143,569	INS-IGF2 IGF2 IGF2-AS
rs1003483(G;T)	11	2,146,313	INS-IGF2 IGF2 IGF2-AS
rs1003483	11	2,146,313	INS-IGF2 IGF2 IGF2-AS
rs1003484	11	2,146,388	INS-IGF2 IGF2 IGF2-AS
rs10770125	11	2,147,784	INS-IGF2 IGF2 IGF2-AS
rs3741211	11	2,147,880	INS-IGF2 IGF2 IGF2-AS
rs3741208	11	2,148,544	INS-IGF2 IGF2 IGF2-AS
rs3741206	11	2,148,634	INS-IGF2 IGF2 IGF2-AS
rs3741205	11	2,148,654	INS-IGF2 IGF2 IGF2-AS
rs3741204	11	2,148,678	INS-IGF2 IGF2 IGF2-AS
rs1004446	11	2,148,913	INS-IGF2 IGF2 IGF2-AS
rs4320932(A;A)	11	2,150,371	INS-IGF2 IGF2	normal
rs4320932	11	2,150,371	INS-IGF2 IGF2
rs4320932(G;G)	11	2,150,371	INS-IGF2 IGF2	0.74x decreased risk for ovarian cancer
rs4320932(A;G)	11	2,150,371	INS-IGF2 IGF2	0.87x decreased risk for ovarian cancer
rs7924316	11	2,152,217	INS-IGF2
rs3842727	11	2,163,618	TH
rs771351747	11	2,164,327	TH
rs771351747(T;T)	11	2,164,327	TH	common in clinvar
rs45471299	11	2,164,339	TH
rs45471299(C;C)	11	2,164,339	TH	common in clinvar
rs2070762	11	2,165,105	TH
rs786204540	11	2,165,284	TH
rs786204540(C;C)	11	2,165,284	TH	common in clinvar
rs11564717	11	2,165,659	TH
rs11564717(C;C)	11	2,165,659	TH	common in clinvar
rs121917762	11	2,165,727	TH
rs121917762(C;C)	11	2,165,727	TH	common in clinvar
rs587776767(A;A)	11	2,165,787	TH	common in clinvar
rs587776767	11	2,165,787	TH
rs587776767(T;T)	11	2,165,787	TH	common in clinvar
rs1057516819	11	2,166,001	TH
rs1057516819(G;G)	11	2,166,001	TH	common in clinvar
rs1057520384	11	2,166,003	TH
rs1057520384(C;C)	11	2,166,003	TH	common in clinvar
rs1057517162(C;C)	11	2,166,530	TH	common in clinvar
rs1057517162	11	2,166,530	TH
rs121917765(G;G)	11	2,166,544	TH	common in clinvar
rs121917765	11	2,166,544	TH
rs1057516736	11	2,166,632	TH
rs1057516736(G;G)	11	2,166,632	TH	common in clinvar
rs1057516491(G;G)	11	2,166,689	TH	common in clinvar
rs1057516491	11	2,166,689	TH
rs28934580	11	2,166,693	TH
rs28934580(C;C)	11	2,166,693	TH
rs28934580(G;G)	11	2,166,693	TH	common in clinvar
rs121917764	11	2,166,762	TH
rs121917764(C;C)	11	2,166,762	TH	common in clinvar
rs28934581(A;A)	11	2,166,995	TH	common in clinvar
rs28934581	11	2,166,995	TH
... further results

Dopamine conversion[edit]

to norepinephrine[edit]

DBH

	On chromosome	Chromosome position	In gene	Summary
rs1611114	9	133,635,081	DBH
rs1611115(C;T)	9	133,635,393	DBH	normal
rs1611115(T;T)	9	133,635,393	DBH	somewhat more associated with impulsiveness and adult ADHD
rs1611115	9	133,635,393	DBH
rs1611115(C;C)	9	133,635,393	DBH	normal
rs267606760	9	133,636,672	DBH
rs267606760(G;G)	9	133,636,672	DBH	common in clinvar
rs74853476	9	133,636,712	DBH
rs74853476(T;T)	9	133,636,712	DBH	common in clinvar
rs3025382	9	133,637,199	DBH
rs2007153(A;G)	9	133,638,697	DBH	normal risk of schizophrenia in limited study
rs2007153(G;G)	9	133,638,697	DBH	increased risk of schizophrenia in limited study
rs2007153	9	133,638,697	DBH
rs2007153(A;A)	9	133,638,697	DBH	decreased risk of schizophrenia in limited study
rs77576840	9	133,639,848	DBH
rs77576840(C;C)	9	133,639,848	DBH	common in clinvar
rs1108580	9	133,639,992	DBH
rs1108580(A;A)	9	133,639,992	DBH	common in clinvar
rs863225244(A;A)	9	133,642,337	DBH	common in clinvar
rs863225244	9	133,642,337	DBH
rs5320(G;G)	9	133,642,351	DBH	common in complete genomics
rs5320	9	133,642,351	DBH
rs863225245	9	133,643,474	DBH
rs863225245(G;G)	9	133,643,474	DBH	common in clinvar
rs1611125	9	133,644,190	DBH
rs4531	9	133,644,248	DBH
rs4531(G;G)	9	133,644,248	DBH	common on affy axiom data
rs2519152	9	133,644,512	DBH
rs267606761	9	133,647,854	DBH
rs267606761(G;G)	9	133,647,854	DBH	common in clinvar
rs75215331(C;C)	9	133,647,906	DBH	common in clinvar
rs75215331	9	133,647,906	DBH
rs2283123(T;T)	9	133,650,175	DBH	decreased risk of schizophrenia in limited study
rs2283123	9	133,650,175	DBH
rs2283123(C;C)	9	133,650,175	DBH	normal risk of schizophrenia in limited study
rs2283123(C;T)	9	133,650,175	DBH	decreased risk of schizophrenia in limited study
rs739398	9	133,651,448	DBH
rs77905(T;T)	9	133,652,975	DBH	common in clinvar
rs77905	9	133,652,975	DBH
rs6271(C;C)	9	133,657,152	DBH DBH-AS1	common in clinvar
rs6271	9	133,657,152	DBH DBH-AS1
rs863225246	9	133,657,174	DBH DBH-AS1
rs863225246(A;A)	9	133,657,174	DBH DBH-AS1	common in clinvar
rs129882(C;C)	9	133,658,547	DBH DBH-AS1	common in clinvar
rs129882	9	133,658,547	DBH DBH-AS1
rs761334309	9	135,503,570	LOC101928525 MRPS2
rs761334309(C;C)	9	135,503,570	LOC101928525 MRPS2	common/normal
rs761334309(C;T)	9	135,503,570	LOC101928525 MRPS2	Carrier of a combined oxidative phosphorylation deficiency-36 mutation
rs201229537	9	135,503,582	LOC101928525 MRPS2
rs758539748	9	135,503,655	LOC101928525 MRPS2

Dopamine degradation[edit]

COMT

	On chromosome	Chromosome position	In gene	Summary
rs2097603	22	19,940,569	COMT TXNRD2
rs2075507	22	19,940,569	COMT TXNRD2
rs2020917	22	19,941,361	COMT TXNRD2
rs13306278(C;C)	22	19,941,504	COMT TXNRD2	common in clinvar
rs13306278	22	19,941,504	COMT TXNRD2
rs737866	22	19,942,586	COMT TXNRD2
rs737865(A;G)	22	19,942,598	COMT TXNRD2
rs737865	22	19,942,598	COMT TXNRD2
rs933271	22	19,943,884	COMT TXNRD2
rs5993882	22	19,950,010	COMT
rs3087869	22	19,953,984	COMT
rs740603	22	19,957,654	COMT
rs4646312	22	19,960,814	COMT
rs165656	22	19,961,340	COMT
rs165722	22	19,961,490	COMT
rs6269	22	19,962,429	COMT MIR4761
rs4633(T;T)	22	19,962,712	COMT MIR4761	higher risk for endometrial cancer
rs4633(C;T)	22	19,962,712	COMT MIR4761	higher risk for endometrial cancer
rs4633(C;C)	22	19,962,712	COMT MIR4761	normal
rs4633	22	19,962,712	COMT MIR4761
rs6267	22	19,962,740	COMT MIR4761
rs6267(G;G)	22	19,962,740	COMT MIR4761	common
rs6267(G;T)	22	19,962,740	COMT MIR4761	None
rs6267(T;T)	22	19,962,740	COMT MIR4761	None
rs740602	22	19,962,745	COMT MIR4761
rs740602(G;G)	22	19,962,745	COMT MIR4761	common in complete genomics
rs2239393	22	19,962,905	COMT MIR4761
rs4818	22	19,963,684	COMT MIR4761
rs4818(C;C)	22	19,963,684	COMT MIR4761	common in clinvar
rs4818(C;G)	22	19,963,684	COMT MIR4761
rs8192488	22	19,963,714	COMT MIR4761
rs8192488(C;C)	22	19,963,714	COMT MIR4761	common in complete genomics
rs17849308	22	19,963,748	COMT MIR4761
rs4680(G;G)	22	19,963,748	COMT MIR4761	(warrior) multiple associations, see details
rs4680(A;A)	22	19,963,748	COMT MIR4761	(worrier) advantage in memory and attention tasks
rs4680(A;G)	22	19,963,748	COMT MIR4761	Intermediate dopamine levels, other effects
rs165688(G;G)	22	19,963,748	COMT MIR4761
rs4680	22	19,963,748	COMT MIR4761	warrior vs worrier; number of other associations
rs165688	22	19,963,748	COMT MIR4761
rs769224	22	19,964,281	COMT MIR4761
rs769224(G;G)	22	19,964,281	COMT MIR4761
rs165631(C;T)	22	19,964,293	COMT MIR4761	Perhaps slightly lower risk for breast cancer in BRCA1/2 mutation carriers?
rs165631	22	19,964,293	COMT MIR4761
rs165631(C;C)	22	19,964,293	COMT MIR4761	common/normal
rs4646316	22	19,964,609	COMT
rs165774	22	19,965,038	COMT
rs9332377(C;C)	22	19,968,169	COMT ARVCF	common/normal
rs9332377	22	19,968,169	COMT ARVCF
rs165599(A;G)	22	19,969,258	COMT ARVCF
rs165599(A;A)	22	19,969,258	COMT ARVCF
... further results

MAOA

	On chromosome	Chromosome position	In gene	Summary
rs5953210	X	43,654,798	MAOA
rs3788862	X	43,658,116	MAOA
rs5906883	X	43,667,695	MAOA
rs1465107	X	43,678,769	MAOA
rs796065312	X	43,683,572	MAOA
rs796065312(C;C)	X	43,683,572	MAOA	common in clinvar
rs5906957	X	43,688,062	MAOA
rs909525(A;A)	X	43,693,955	MAOA	Probably MAOA 4 or 5 repeats: not Warrior Gene.
rs909525(G;G)	X	43,693,955	MAOA	Perhaps MAOA 3 repeats: Warrior Gene?
rs909525(A;G)	X	43,693,955	MAOA	Probably one Warrior Gene and one non-Warrior Gene.
rs909525	X	43,693,955	MAOA	Best proxy for Warrior Gene repeats.
rs2283725	X	43,700,729	MAOA
rs796065311(-;-)	X	43,731,344	MAOA	common in clinvar
rs796065311	X	43,731,344	MAOA
rs587777457(G;G)	X	43,731,695	MAOA	common in clinvar
rs587777457	X	43,731,695	MAOA
rs72554632(C;T)	X	43,731,784	MAOA	Carrier for Brunner's Syndrome
rs72554632	X	43,731,784	MAOA
rs72554632(C;C)	X	43,731,784	MAOA	common in clinvar
rs72554632(T;T)	X	43,731,784	MAOA	possible mental retardation
rs6323	X	43,731,789	MAOA	Monoamine oxidase A activity
rs6323(G;G)	X	43,731,789	MAOA	Increased monoamine oxidase A activity
rs6323(T;T)	X	43,731,789	MAOA	reduced MAOA activity
rs3027400	X	43,733,516	MAOA
rs2235186	X	43,736,181	MAOA
rs2072743	X	43,740,274	MAOA
rs979606	X	43,741,895	MAOA
rs1137070	X	43,744,144	MAOA
rs3027407	X	43,745,594	MAOA
rs3027409	X	43,747,786	MAOA
rs3027409(T;T)	X	43,747,786	MAOA	common on affy axiom data
rs6609257	X	43,753,461	MAOA

MAOB

	On chromosome	Chromosome position	In gene
rs3027415	X	43,755,194	MAOB
rs3027415(T;T)	X	43,755,194	MAOB
rs1799836	X	43,768,752	MAOB
rs1799836(C;C)	X	43,768,752	MAOB
rs10521432	X	43,774,493	MAOB
rs2283729	X	43,818,795	MAOB
rs6651806	X	43,829,718	MAOB

Dopamine transporters[edit]

SLC6A3/DAT

	On chromosome	Chromosome position	In gene	Summary
rs3863145	5	1,392,596	SLC6A3
rs28363170	5	1,393,747	SLC6A3
rs28363170(-;-)	5	1,393,747	SLC6A3
rs27072(T;T)	5	1,394,407	SLC6A3	Lower risk of alcohol withdrawal seizures, and probably lower odds of ADHD.
rs27072(C;T)	5	1,394,407	SLC6A3	Lower risk of alcohol withdrawal seizures, and perhaps lower odds of ADHD.
rs27072(C;C)	5	1,394,407	SLC6A3	2x risk of severe alcohol withdrawal. Possible increased odds of ADHD.
rs27072	5	1,394,407	SLC6A3	Associated with increased susceptibility to alcohol withdrawal symptoms and ADHD.
rs40184	5	1,394,962	SLC6A3
rs6869645(C;C)	5	1,404,433	SLC6A3	common in complete genomics
rs6869645	5	1,404,433	SLC6A3
rs431905516	5	1,406,226	SLC6A3
rs431905516(T;T)	5	1,406,226	SLC6A3	Infantile Parkinsonism-dystonia
rs431905516(C;T)	5	1,406,226	SLC6A3	Carrier of an infantile Parkinsonism-dystonia mutation
rs431905516(C;C)	5	1,406,226	SLC6A3	common in clinvar
rs431905504(A;A)	5	1,411,242	SLC6A3	Infantile Parkinsonism-dystonia
rs431905504(G;G)	5	1,411,242	SLC6A3	common in clinvar
rs431905504(A;G)	5	1,411,242	SLC6A3	Carrier of an infantile Parkinsonism-dystonia mutation
rs431905504	5	1,411,242	SLC6A3
rs6347(A;A)	5	1,411,297	SLC6A3	common in clinvar
rs6347	5	1,411,297	SLC6A3
rs267607069(T;T)	5	1,411,328	SLC6A3	Infantile Parkinsonism-dystonia
rs267607069(C;T)	5	1,411,328	SLC6A3	Carrier of an infantile Parkinsonism-dystonia mutation
rs267607069	5	1,411,328	SLC6A3
rs267607069(C;C)	5	1,411,328	SLC6A3	common in clinvar
rs3836790(-;-)	5	1,411,740	SLC6A3	common in complete genomics
rs3836790	5	1,411,740	SLC6A3
rs27048(C;C)	5	1,412,530	SLC6A3	2x risk of severe alcohol withdrawal
rs27048(C;T)	5	1,412,530	SLC6A3	normal
rs27048(T;T)	5	1,412,530	SLC6A3	normal
rs27048	5	1,412,530	SLC6A3
rs267607068	5	1,414,744	SLC6A3
rs267607068(T;T)	5	1,414,744	SLC6A3	common in clinvar
rs267607068(A;A)	5	1,414,744	SLC6A3	Infantile Parkinsonism-dystonia
rs267607068(A;T)	5	1,414,744	SLC6A3	Carrier of an infantile Parkinsonism-dystonia mutation
rs37022(T;T)	5	1,415,514	SLC6A3	common in complete genomics
rs37022	5	1,415,514	SLC6A3
rs431905514(A;G)	5	1,416,097	SLC6A3	Carrier of an infantile Parkinsonism-dystonia mutation
rs431905514	5	1,416,097	SLC6A3
rs431905514(A;A)	5	1,416,097	SLC6A3	Infantile Parkinsonism-dystonia
rs431905514(G;G)	5	1,416,097	SLC6A3	common in clinvar
rs431905515	5	1,421,997	SLC6A3
rs431905515(C;C)	5	1,421,997	SLC6A3	Infantile Parkinsonism-dystonia
rs431905515(T;T)	5	1,421,997	SLC6A3	common in clinvar
rs431905515(C;T)	5	1,421,997	SLC6A3	Carrier of an infantile Parkinsonism-dystonia mutation
rs464049(C;C)	5	1,423,790	SLC6A3	decreased risk of schizophrenia in limited study
rs464049(C;T)	5	1,423,790	SLC6A3	increased risk of schizophrenia in limited study
rs464049(T;T)	5	1,423,790	SLC6A3	increased risk of schizophrenia in limited study
rs464049	5	1,423,790	SLC6A3
rs10052016	5	1,427,996	SLC6A3
rs463379	5	1,431,049	SLC6A3
... further results

SLC18A2/VMAT2

	On chromosome	Chromosome position	In gene	Summary
rs60912143	10	117,241,017	SLC18A2 LOC105378500
rs363387	10	117,244,053	SLC18A2 LOC105378500
rs363387(T;T)	10	117,244,053	SLC18A2 LOC105378500
rs1060499741	10	117,255,281	SLC18A2
rs1060499741(C;C)	10	117,255,281	SLC18A2	common in clinvar
rs2015586	10	117,262,226	SLC18A2
rs363224(A;A)	10	117,263,062	SLC18A2	Protective against TD occurrence
rs363224	10	117,263,062	SLC18A2
rs363227	10	117,267,055	SLC18A2
rs363276	10	117,274,298	SLC18A2

Dopamine receptors[edit]

D1-like[edit]

DRD1

	On chromosome	Chromosome position	In gene	Summary
rs11746641	5	175,439,088	DRD1
rs11749676	5	175,439,295	DRD1
rs686	5	175,441,697	DRD1
rs686(G;G)	5	175,441,697	DRD1
rs155417(C;C)	5	175,441,837	DRD1	common in complete genomics
rs155417	5	175,441,837	DRD1
rs1799914(G;G)	5	175,442,902	DRD1	common in complete genomics
rs1799914	5	175,442,902	DRD1
rs4532	5	175,443,147	DRD1
rs4532(C;C)	5	175,443,147	DRD1
rs5326	5	175,443,193	DRD1
rs5326(A;G)	5	175,443,193	DRD1	possible psychiatric risks
rs265981(A;A)	5	175,443,899	DRD1
rs265981	5	175,443,899	DRD1

DRD5

	On chromosome	Chromosome position	In gene	Summary
rs2227852	4	9,782,741	SLC2A9 DRD5
rs2227852(A;A)	4	9,782,741	SLC2A9 DRD5
rs2227852(G;G)	4	9,782,741	SLC2A9 DRD5	common for caucasians, despite hapmap
rs6283	4	9,783,007	SLC2A9 DRD5
rs1967550	4	9,783,641	SLC2A9 DRD5

D2-like[edit]

DRD2

	On chromosome	Chromosome position	In gene	Summary
rs2234689	11	113,407,761	DRD2
rs1554929	11	113,408,042	DRD2
rs2242592	11	113,408,708	DRD2
rs2734842	11	113,409,552	DRD2
rs6279	11	113,410,351	DRD2
rs6276	11	113,410,675	DRD2
rs2734841	11	113,411,054	DRD2
rs1124493	11	113,411,573	DRD2
rs6277(C;C)	11	113,412,737	DRD2	1.6x higher schizophrenia risk
rs6277(C;T)	11	113,412,737	DRD2	1.4x higher schizophrenia risk
rs6277	11	113,412,737	DRD2
rs6277(T;T)	11	113,412,737	DRD2	normal schizophrenia risk, learns NoGo faster
rs6275(T;T)	11	113,412,755	DRD2	common in clinvar
rs6275	11	113,412,755	DRD2
rs1801028	11	113,412,762	DRD2
rs1801028(C;G)	11	113,412,762	DRD2	1.4x risk for schizophrenia
rs1801028(C;C)	11	113,412,762	DRD2	normal risk
rs1801028(G;G)	11	113,412,762	DRD2	normal risk
rs1800496	11	113,412,766	DRD2
rs1800496(C;C)	11	113,412,766	DRD2	common in complete genomics
rs1076560(A;A)	11	113,412,966	DRD2	influences working memory
rs1076560(A;C)	11	113,412,966	DRD2	1.3x increased risk for alcoholism
rs1076560(C;C)	11	113,412,966	DRD2	normal
rs1076560	11	113,412,966	DRD2
rs2283265	11	113,414,814	DRD2
rs12363125	11	113,415,194	DRD2
rs2734839	11	113,415,768	DRD2
rs104894220	11	113,416,935	DRD2
rs104894220(G;G)	11	113,416,935	DRD2	common in clinvar
rs1079727	11	113,418,460	DRD2
rs1800498	11	113,420,866	DRD2
rs2075652	11	113,424,176	DRD2
rs1076562	11	113,425,286	DRD2
rs1079598	11	113,425,552	DRD2
rs1079597	11	113,425,564	DRD2
rs1079596	11	113,425,897	DRD2
rs1125394	11	113,426,463	DRD2
rs4436578	11	113,436,043	DRD2
rs11214606(C;C)	11	113,439,147	DRD2	common on affy axiom data
rs11214606	11	113,439,147	DRD2
rs4648318	11	113,442,667	DRD2
rs4648319	11	113,443,641	DRD2
rs17601612	11	113,447,023	DRD2
rs7131056	11	113,459,052	DRD2
rs4648317(T;T)	11	113,460,810	DRD2	prone to higher nicotine dependence, more impulsive/sensation seeking
rs4648317(C;C)	11	113,460,810	DRD2	normal
rs4648317	11	113,460,810	DRD2
rs4648317(C;T)	11	113,460,810	DRD2	prone to higher nicotine dependence?
rs11214613	11	113,464,537	DRD2
rs11214613(G;G)	11	113,464,537	DRD2	common in complete genomics
... further results

DRD3

	On chromosome	Chromosome position	In gene	Summary
rs2399496	3	114,127,166	DRD3
rs9868039	3	114,127,695	DRD3
rs4646996	3	114,130,718	DRD3
rs2134655	3	114,139,354	DRD3
rs2251177(C;C)	3	114,139,503	DRD3	common in clinvar
rs2251177	3	114,139,503	DRD3
rs201252087	3	114,142,742	DRD3
rs963468	3	114,144,040	DRD3
rs3773679	3	114,150,488	DRD3
rs3773678	3	114,151,231	DRD3
rs2630349	3	114,154,525	DRD3
rs2630349(G;G)	3	114,154,525	DRD3	common in complete genomics
rs2630351	3	114,156,212	DRD3
rs2630351(G;G)	3	114,156,212	DRD3	common in complete genomics
rs167771(G;G)	3	114,157,428	DRD3
rs167771(A;A)	3	114,157,428	DRD3
rs167771	3	114,157,428	DRD3	Individuals carrying the AA variant of the rs167771 SNP scored significantly higher on the IS-factor (resp U = 590, p < .01), indicating more rigid behavior than individuals carrying one or two copies of the minor G-allele.
rs324032	3	114,158,981	DRD3
rs324032(A;A)	3	114,158,981	DRD3	common in complete genomics
rs167770	3	114,160,715	DRD3
rs324029	3	114,162,776	DRD3
rs3732783	3	114,171,942	DRD3
rs3732783(A;A)	3	114,171,942	DRD3	common in clinvar
rs6280(C;C)	3	114,171,968	DRD3	better response to olanzapine
rs6280(T;T)	3	114,171,968	DRD3	normal
rs6280(C;T)	3	114,171,968	DRD3	normal
rs6280	3	114,171,968	DRD3
rs9825563	3	114,181,373	DRD3

DRD4

	On chromosome	Chromosome position	In gene	Summary
rs3758653	11	636,399	DRD4
rs747302	11	636,689	DRD4
rs936462	11	636,690	DRD4
rs1800955(C;C)	11	636,784	DRD4	increased susceptibility to novelty seeking
rs1800955(T;T)	11	636,784	DRD4	normal
rs1800955(C;T)	11	636,784	DRD4	increased susceptibility to novelty seeking
rs1800955	11	636,784	DRD4	influences personality
rs916457	11	637,014	DRD4
rs916457(C;C)	11	637,014	DRD4
rs554375713	11	637,537	DRD4
rs587776842(GCCGACCTCCTCC;GCCGACCTCCTCC)	11	637,539	DRD4	common in clinvar
rs587776842	11	637,539	DRD4
rs587776842(CCGCCGACCTCCT;CCGCCGACCTCCT)	11	637,539	DRD4	common in clinvar
rs587776842(-;GCCGACCTCCTCC)	11	637,539	DRD4	Carrier of DRD4 deletion allele
rs587776842(-;-)	11	637,539	DRD4	Autonomic nervous system dysfunction?
rs752306	11	637,622	DRD4
rs12720390	11	637,932	DRD4
rs12720403	11	639,274	DRD4
rs1800443	11	639,830	DRD4
rs1800443(T;T)	11	639,830	DRD4	common in clinvar
rs1800443(G;T)	11	639,830	DRD4	Uncommon DRD4 polymorphism
rs1800443(G;G)	11	639,830	DRD4	Rare DRD4 polymorphism
rs762502	11	640,119	DRD4
rs12720410	11	640,254	DRD4
rs936463	11	640,432	DRD4
rs11246226(C;C)	11	641,191	DRD4	decreased risk of schizophrenia in limited study
rs11246226(A;A)	11	641,191	DRD4	increased risk of schizophrenia in limited study
rs11246226	11	641,191	DRD4
rs11246226(A;C)	11	641,191	DRD4	decreased risk of schizophrenia in limited study
rs4331145(G;G)	11	643,683	DRD4	increased risk of schizophrenia in limited study
rs4331145	11	643,683	DRD4
rs4331145(A;A)	11	643,683	DRD4	increased risk of schizophrenia in limited study
rs4331145(A;G)	11	643,683	DRD4	decreased risk of schizophrenia in limited study

Dopamine/all

Contents

Dopamine synthesis[edit]

Dopamine conversion[edit]

to norepinephrine[edit]

Dopamine degradation[edit]

Dopamine transporters[edit]

Dopamine receptors[edit]

D1-like[edit]

D2-like[edit]