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rs1044397

From SNPedia

Orientationminus
Stabilizedplus
Make rs1044397(A;A)
Make rs1044397(A;G)
Make rs1044397(G;G)
ReferenceGRCh38 38.1/142
Chromosome20
Position63349752
GeneCHRNA4
is asnp
is mentioned by
dbSNPrs1044397
ebirs1044397
HLIrs1044397
Exacrs1044397
Varsomers1044397
Maprs1044397
PheGenIrs1044397
hapmaprs1044397
1000 genomesrs1044397
hgdprs1044397
ensemblrs1044397
gopubmedrs1044397
geneviewrs1044397
scholarrs1044397
googlers1044397
pharmgkbrs1044397
gwascentralrs1044397
openSNPrs1044397
23andMers1044397
23andMe allrs1044397
SNP Nexus

SNPshotrs1044397
SNPdbers1044397
MSV3drs1044397
GWAS Ctlgrs1044397
GMAF0.3958
Max Magnitude
OMIM118504
DescCHOLINERGIC RECEPTOR, NEURONAL NICOTINIC, ALPHA POLYPEPTIDE 4; CHRNA4
Variant0006
Relatedalso
OMIM118504
Desc
Variant0006
Relatedalso
[PMID 15154117OA-icon.png] A common haplotype of the nicotine acetylcholine receptor alpha 4 subunit gene is associated with vulnerability to nicotine addiction in men.


[PMID 17135278OA-icon.png] Cholinergic nicotinic receptor genes implicated in a nicotine dependence association study targeting 348 candidate genes with 3713 SNPs.


[PMID 18571741OA-icon.png] Genetic variability in nicotinic acetylcholine receptors and nicotine addiction: converging evidence from human and animal research.


[PMID 18618000OA-icon.png] A candidate gene approach identifies the CHRNA5-A3-B4 region as a risk factor for age-dependent nicotine addiction.


[PMID 18698231OA-icon.png] Polymorphisms affecting gene transcription and mRNA processing in pharmacogenetic candidate genes: detection through allelic expression imbalance in human target tissues.


[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.


[PMID 19693267OA-icon.png] Financial and psychological risk attitudes associated with two single nucleotide polymorphisms in the nicotine receptor (CHRNA4) gene.


ClinVar
Risk rs1044397(A;A)
Alt rs1044397(A;A)
Reference rs1044397(G;G)
Significance Other
Disease not specified
Variation info
Gene CHRNA4
CLNDBN not specified
Reversed 1
HGVS NC_000020.10:g.61981104C>T
CLNSRC ClinVar Emory University University of Chicago
CLNACC RCV000079314.7,