Gene: PTPN22 ×
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
0.020 GeneticVariation BEFREE Lack of association between the protein tyrosine phosphatase non-receptor type 22 R263Q and R620W functional genetic variants and endogenous non-anterior uveitis. 23559857

2013
dbSNP: rs2476601
rs2476601
PTPN22 ; AP4B1-AS1
0.020 GeneticVariation BEFREE By contrast, PTPN22 C1858T showed a negligible association with systemic sclerosis, celiac disease, multiple sclerosis, psoriasis, ankylosing spondylitis, pemphigus vulgaris, ulcerative colitis, primary sclerosing cholangitis, primary biliary cirrhosis, Crohn's disease and acute anterior uveitis. 23076337

2012
dbSNP: rs33996649
rs33996649
PTPN22 ; AP4B1-AS1
0.010 GeneticVariation BEFREE Lack of association between the protein tyrosine phosphatase non-receptor type 22 R263Q and R620W functional genetic variants and endogenous non-anterior uveitis. 23559857

2013