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rs1044394

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in complete genomics
(T;T) 0 common in clinvar
Make rs1044394(C;T)
ReferenceGRCh38 38.1/142
Chromosome20
Position63350733
GeneCHRNA4
is asnp
is mentioned by
dbSNPrs1044394
ebirs1044394
HLIrs1044394
Exacrs1044394
Varsomers1044394
Maprs1044394
PheGenIrs1044394
hapmaprs1044394
1000 genomesrs1044394
hgdprs1044394
ensemblrs1044394
gopubmedrs1044394
geneviewrs1044394
scholarrs1044394
googlers1044394
pharmgkbrs1044394
gwascentralrs1044394
openSNPrs1044394
23andMers1044394
23andMe allrs1044394
SNP Nexus

SNPshotrs1044394
SNPdbers1044394
MSV3drs1044394
GWAS Ctlgrs1044394
GMAF0.1276
Max Magnitude0
? (C;C) (C;T) (T;T) 28

[PMID 19482438] Association of genes coding for the alpha-4, alpha-5, beta-2 and beta-3 subunits of nicotinic receptors with cigarette smoking and nicotine dependence


[PMID 17613539] Association of attentional network function with exon 5 variations of the CHRNA4 gene.


[PMID 21445957OA-icon.png] Association of CHRNA4 polymorphisms with smoking behavior in two populations.


[PMID 23350800OA-icon.png] Nominal association with CHRNA4 variants and nicotine dependence.


ClinVar
Risk rs1044394(C;C)
Alt rs1044394(C;C)
Reference rs1044394(T;T)
Significance Probable-non-pathogenic
Disease not specified
Variation info
Gene CHRNA4
CLNDBN not specified
Reversed 1
HGVS NC_000020.10:g.61982085A>G
CLNSRC ClinVar University of Chicago
CLNACC RCV000116723.2,