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 The PTPN22 R620W minor allele is associated with susceptibility to IIM in SA patients, independent of the 8.1 AH. 27312665

2017
dbSNP: rs2476601
rs2476601
PTPN22 ; AP4B1-AS1
0.020 GeneticVariation BEFREE The R620W variant is a significant risk factor for IIM, independent of the HLA 8.1 haplotype. 18821667

2008
dbSNP: rs6590330
rs6590330 		0.010 GeneticVariation BEFREE Additionally, the rs6590330 genotype was associated with IIMs (P <sub>c</sub>  = 0.020).</span> 29030598

2017
dbSNP: rs7117932
rs7117932
ETS1 ; LOC105369565
0.010 GeneticVariation BEFREE Our data indicated that the rs7117932 alleles and genotypes are associated with DM and IIMs (P <sub>c</sub>  = 6.0 × 10<sup>-3</sup> and P <sub>c</sub>  = 0.029; P <sub>c</sub>  = 0.013 and P <sub>c</sub>  = 0.019, respectively). 29030598

2017
dbSNP: rs2071592
rs2071592
ATP6V1G2 ; NFKBIL1 ; ATP6V1G2-DDX39B
0.010 GeneticVariation BEFREE A significant allele association was observed in the overall IIM group vs controls for the IKBL-62T allele (rs2071592, odds ratio 1.5, 95% CI 1.21, 1.89, corrected P = 0.0086), which strengthened after stratification by anti-Jo-1 or -PM-Scl antibodies. 22210660

2012