Source: ALL
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 0.93 121
rs6590330 0.851 0.280 11 128441164 intergenic variant G/A;T snv 5
rs2071592
ATP6V1G2-DDX39B ; ATP6V1G2 ; NFKBIL1
0.882 0.200 6 31547563 intron variant T/A;C snv 3
rs7117932
ETS1 ; LOC105369565
1.000 0.080 11 128567058 intron variant C/T snv 0.37 2