rs9851967
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | normal | |
(C;T) | 0.88x risk of vitiligo in Chinese | |
(T;T) | 0.88x risk of vitiligo in Chinese |
Reference | GRCh38 38.1/141 |
Chromosome | 3 |
Position | 188369840 |
Gene | LPP |
is a | snp |
is | mentioned by |
dbSNP | rs9851967 |
dbSNP (classic) | rs9851967 |
ClinGen | rs9851967 |
ebi | rs9851967 |
HLI | rs9851967 |
Exac | rs9851967 |
Gnomad | rs9851967 |
Varsome | rs9851967 |
LitVar | rs9851967 |
Map | rs9851967 |
PheGenI | rs9851967 |
Biobank | rs9851967 |
1000 genomes | rs9851967 |
hgdp | rs9851967 |
ensembl | rs9851967 |
geneview | rs9851967 |
scholar | rs9851967 |
rs9851967 | |
pharmgkb | rs9851967 |
gwascentral | rs9851967 |
openSNP | rs9851967 |
23andMe | rs9851967 |
SNPshot | rs9851967 |
SNPdbe | rs9851967 |
MSV3d | rs9851967 |
GWAS Ctlg | rs9851967 |
GMAF | 0.3186 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 22951725] |
Trait | Vitiligo |
Title | Association analyses identify three susceptibility Loci for vitiligo in the Chinese Han population. |
Risk Allele | |
P-val | 9E-8 |
Odds Ratio | 1.14 [1.09-1.19] |
[PMID 18311140] Newly identified genetic risk variants for celiac disease related to the immune response.