Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2476601
rs2476601
PTPN22 ; AP4B1-AS1
0.030 GeneticVariation BEFREE The aim of this study was to test genetic association of the PTPN22 1858C>T variant and generalized vitiligo in a Romanian case-control cohort. 18426414

2008
dbSNP: rs2476601
rs2476601
PTPN22 ; AP4B1-AS1
0.030 GeneticVariation BEFREE The PTPN22 1858T allele of SNP rs2476601 is significantly associated both with generalized vitiligo and with an expanded autoimmunity phenotype. 18200060

2008
dbSNP: rs2476601
rs2476601
PTPN22 ; AP4B1-AS1
0.030 GeneticVariation BEFREE The results indicate that the LYP missense R620W polymorphism may have an influence on the development of generalised vitiligo and provide further evidence for autoimmunity as an aetiological factor with respect to this disease. 16015369

2005