Source: ALL

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs12301088
rs12301088
IFNG-AS1
CUI: C0042900
Disease: Vitiligo
Vitiligo 		0.010 GeneticVariation BEFREE The strongest involved SNPs rs12301088 (near IL26 gene), that was associated with familial vitiligo and existence of halo nevi, and rs2257167 (IFNAR1 gene), that was associated with female vitiligo. 26429320

2016