Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1799983 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs1800629
TNF
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 169
rs2070600 0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 82
rs1800796 0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02 74
rs1800450 0.662 0.640 10 52771475 missense variant C/T snv 0.14 0.11 26
rs7096206 0.708 0.480 10 52771925 upstream gene variant G/A;C;T snv 17
rs1799946 0.732 0.360 8 6877909 5 prime UTR variant C/T snv 0.36 0.41 13
rs61330082 0.732 0.320 7 106286419 upstream gene variant G/A snv 0.22 13
rs4957796
FER
0.851 0.120 5 109066439 intron variant T/C snv 0.16 5
rs11137480 0.882 0.120 9 88989662 upstream gene variant G/C snv 0.37 3
rs2664581
PI3
0.882 0.120 20 45175881 missense variant A/C snv 0.16 0.16 3
rs7022797 0.882 0.120 9 88989548 upstream gene variant T/G snv 0.38 3