Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs8192917
rs8192917
GZMB ; LOC107984667
0.810 GeneticVariation BEFREE The SNP rs8192917, a non-synonymous coding SNP, was identified to be significantly associated with the disease status of vitiligo, with OR = 1.39 and P = 1.92 × 10<sup>-8</sup>. 30158536

2018
dbSNP: rs8192917
rs8192917
GZMB ; LOC107984667
C 0.810 GeneticVariation GWASCAT Genome-wide association studies of autoimmune vitiligo identify 23 new risk loci and highlight key pathways and regulatory variants. 27723757

2016
dbSNP: rs8192917
rs8192917
GZMB ; LOC107984667
0.810 GeneticVariation GWASDB Genome-wide association analyses identify 13 new susceptibility loci for generalized vitiligo. 22561518

2012
dbSNP: rs8192917
rs8192917
GZMB ; LOC107984667
G 0.810 GeneticVariation GWASCAT Variant of TYR and autoimmunity susceptibility loci in generalized vitiligo. 20410501

2010
dbSNP: rs8192917
rs8192917
GZMB ; LOC107984667
G 0.810 GeneticVariation GWASDB Variant of TYR and autoimmunity susceptibility loci in generalized vitiligo. 20410501

2010