rs13208776, SMOC2

N. diseases: 3
Disease: Generalized vitiligo ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Generalized vitiligo
CUI: C1304470
Disease: Generalized vitiligo
0.010 GeneticVariation BEFREE The region of association contains only one gene, SMOC2, within which SNP rs13208776 attained genome-wide significance for association with generalized vitiligo (P=8.51x10(-8)) at odds ratio 7.445 (95% confidence interval=3.56-15.53) for the high-risk allele and population attributable risk 28.00. 19890347 2010