Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs4986790 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs1800629
TNF
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 169
rs20541 0.585 0.720 5 132660272 missense variant A/G snv 0.72 0.77 52
rs1800925 0.627 0.560 5 132657117 non coding transcript exon variant C/G;T snv 37
rs2070874
IL4
0.672 0.560 5 132674018 5 prime UTR variant C/T snv 0.28 0.28 27
rs10767664 0.752 0.400 11 27704439 intron variant T/A snv 0.83 16
rs8076131 0.790 0.200 17 39924659 intron variant G/A;C snv 11