rs59374417
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs59374417(A;A) |
Make rs59374417(A;C) |
Make rs59374417(C;C) |
Reference | GRCh38 38.1/141 |
Chromosome | 3 |
Position | 119569567 |
is a | snp |
is | mentioned by |
dbSNP | rs59374417 |
dbSNP (classic) | rs59374417 |
ClinGen | rs59374417 |
ebi | rs59374417 |
HLI | rs59374417 |
Exac | rs59374417 |
Gnomad | rs59374417 |
Varsome | rs59374417 |
LitVar | rs59374417 |
Map | rs59374417 |
PheGenI | rs59374417 |
Biobank | rs59374417 |
1000 genomes | rs59374417 |
hgdp | rs59374417 |
ensembl | rs59374417 |
geneview | rs59374417 |
scholar | rs59374417 |
rs59374417 | |
pharmgkb | rs59374417 |
gwascentral | rs59374417 |
openSNP | rs59374417 |
23andMe | rs59374417 |
SNPshot | rs59374417 |
SNPdbe | rs59374417 |
MSV3d | rs59374417 |
GWAS Ctlg | rs59374417 |
GMAF | 0.1942 |
Max Magnitude | 0 |
GWAS snp | |
---|---|
PMID | [PMID 22561518![]() |
Trait | |
Title | Genome-wide association analyses identify 13 new susceptibility loci for generalized vitiligo. |
Risk Allele | C |
P-val | 4E-10 |
Odds Ratio | 1.3400 None |