Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs11966200
rs11966200
CYP21A2 ; SLC44A4
0.810 GeneticVariation BEFREE The study suggested that the underlying risk causal allele tagged by SNP rs11966200 might not only play important roles in the development of vitiligo, but also contribute to the diverse clinical characteristics of generalized vitiligo at least in Chinese Han population. 23516070

2013
dbSNP: rs11966200
rs11966200
CYP21A2 ; SLC44A4
A 0.810 GeneticVariation GWASDB Genome-wide association study for vitiligo identifies susceptibility loci at 6q27 and the MHC. 20526339

2010
dbSNP: rs11966200
rs11966200
CYP21A2 ; SLC44A4
A 0.810 GeneticVariation GWASCAT Genome-wide association study for vitiligo identifies susceptibility loci at 6q27 and the MHC. 20526339

2010