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rs9851967

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) normal
(C;T) 0.88x risk of vitiligo in Chinese
(T;T) 0.88x risk of vitiligo in Chinese
ReferenceGRCh38 38.1/141
Chromosome3
Position188369840
GeneLPP
is asnp
is mentioned by
dbSNPrs9851967
ebirs9851967
HLIrs9851967
Exacrs9851967
Varsomers9851967
Maprs9851967
PheGenIrs9851967
hapmaprs9851967
1000 genomesrs9851967
hgdprs9851967
ensemblrs9851967
gopubmedrs9851967
geneviewrs9851967
scholarrs9851967
googlers9851967
pharmgkbrs9851967
gwascentralrs9851967
openSNPrs9851967
23andMers9851967
23andMe allrs9851967
SNP Nexus

SNPshotrs9851967
SNPdbers9851967
MSV3drs9851967
GWAS Ctlgrs9851967
GMAF0.3186
Max Magnitude
? (C;C) (C;T) (T;T) 28
Celiac Disease
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 18311140OA-icon.png] Newly identified genetic risk variants for celiac disease related to the immune response.