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rs2302765

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs2302765(A;G)
Make rs2302765(G;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position7447656
GeneCHRNB1
is asnp
is mentioned by
dbSNPrs2302765
ebirs2302765
HLIrs2302765
Exacrs2302765
Varsomers2302765
Maprs2302765
PheGenIrs2302765
hapmaprs2302765
1000 genomesrs2302765
hgdprs2302765
ensemblrs2302765
gopubmedrs2302765
geneviewrs2302765
scholarrs2302765
googlers2302765
pharmgkbrs2302765
gwascentralrs2302765
openSNPrs2302765
23andMers2302765
23andMe allrs2302765
SNP Nexus

SNPshotrs2302765
SNPdbers2302765
MSV3drs2302765
GWAS Ctlgrs2302765
GMAF0.1731
Max Magnitude0
? (A;A) (A;G) (G;G) 28

Variations in this snp have been linked to nicotine dependence [1]


[PMID 17373692OA-icon.png] No evidence for association between 19 cholinergic genes and bipolar disorder.


[PMID 19259974OA-icon.png] Multiple distinct risk loci for nicotine dependence identified by dense coverage of the complete family of nicotinic receptor subunit (CHRN) genes.


ClinVar
Risk rs2302765(G;G)
Alt rs2302765(G;G)
Reference rs2302765(A;A)
Significance Non-pathogenic
Disease not specified
Variation info
Gene CHRNB1
CLNDBN not specified
Reversed 1
HGVS NC_000017.10:g.7350975T>C
CLNSRC ClinVar
CLNACC RCV000116725.1,