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 This is the first report documenting an association between PTPN22 R620W and TA. 30470857

2019
dbSNP: rs2476601
rs2476601
PTPN22 ; AP4B1-AS1
0.020 GeneticVariation BEFREE Totally, 181 patients with TA and 177 healthy controls are genotyped by PCR-RFLP method for the SNP rs2476601 (A/G) of PTPN22 gene. 18375974

2008
dbSNP: rs33996649
rs33996649
PTPN22 ; AP4B1-AS1
0.010 GeneticVariation BEFREE Our data showed that the PTPN22 R620W polymorphism is a risk factor for TA (CC vs. CT: OR 4.3, p = 0.002, and C vs. T: OR 4.1, p = 0.003); however, the PTPN22 R263Q and - 1123G/C polymorphisms are not associated with this AD. 30470857

2019