rs13273442
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs13273442(A;A) |
Make rs13273442(A;G) |
Make rs13273442(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 8 |
Position | 42688874 |
is a | snp |
is | mentioned by |
dbSNP | rs13273442 |
dbSNP (classic) | rs13273442 |
ClinGen | rs13273442 |
ebi | rs13273442 |
HLI | rs13273442 |
Exac | rs13273442 |
Gnomad | rs13273442 |
Varsome | rs13273442 |
LitVar | rs13273442 |
Map | rs13273442 |
PheGenI | rs13273442 |
Biobank | rs13273442 |
1000 genomes | rs13273442 |
hgdp | rs13273442 |
ensembl | rs13273442 |
geneview | rs13273442 |
scholar | rs13273442 |
rs13273442 | |
pharmgkb | rs13273442 |
gwascentral | rs13273442 |
openSNP | rs13273442 |
23andMe | rs13273442 |
SNPshot | rs13273442 |
SNPdbe | rs13273442 |
MSV3d | rs13273442 |
GWAS Ctlg | rs13273442 |
GMAF | 0.3214 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 24401102] Multiple distinct CHRNB3-CHRNA6 variants are genetic risk factors for nicotine dependence in African Americans and European Americans