Disease: Myasthenia Gravis
Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2476601
AP4B1-AS1 ; PTPN22
0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 13
rs2187668
LOC107986589 ; HLA-DQA2 ; HLA-DQA1
0.701 0.480 6 32638107 intron variant C/T snv 3.3E-03 10
rs3129890 0.827 0.280 6 32446496 downstream gene variant T/A;C snv 5
rs1422673
TNIP1
0.925 0.160 5 151059427 intron variant C/G;T snv 2