rs9926296
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs9926296(A;A) |
Make rs9926296(A;G) |
Make rs9926296(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 16 |
Position | 89751681 |
Gene | FANCA |
is a | snp |
is | mentioned by |
dbSNP | rs9926296 |
dbSNP (classic) | rs9926296 |
ClinGen | rs9926296 |
ebi | rs9926296 |
HLI | rs9926296 |
Exac | rs9926296 |
Gnomad | rs9926296 |
Varsome | rs9926296 |
LitVar | rs9926296 |
Map | rs9926296 |
PheGenI | rs9926296 |
Biobank | rs9926296 |
1000 genomes | rs9926296 |
hgdp | rs9926296 |
ensembl | rs9926296 |
geneview | rs9926296 |
scholar | rs9926296 |
rs9926296 | |
pharmgkb | rs9926296 |
gwascentral | rs9926296 |
openSNP | rs9926296 |
23andMe | rs9926296 |
SNPshot | rs9926296 |
SNPdbe | rs9926296 |
MSV3d | rs9926296 |
GWAS Ctlg | rs9926296 |
GMAF | 0.3444 |
Max Magnitude | 0 |
GWAS snp | |
---|---|
PMID | [PMID 22561518![]() |
Trait | |
Title | Genome-wide association analyses identify 13 new susceptibility loci for generalized vitiligo. |
Risk Allele | A |
P-val | 2E-13 |
Odds Ratio | 1.2700 None |