Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1169067903 0.925 0.040 9 131197276 missense variant G/A snv 2
rs778098458 0.925 0.080 10 17229556 missense variant G/A;C snv 1.3E-05 2
rs1131690775 1.000 0.040 4 169590736 missense variant A/C snv 1
rs1131690781 1.000 0.040 21 31668550 missense variant C/A;G snv 1
rs1131690782 1.000 0.040 1 11022452 missense variant G/T snv 1
rs377607698 1.000 0.040 4 169424635 missense variant G/A;C snv 2.4E-05; 4.0E-06 1
rs55824172 1.000 0.040 12 64466994 missense variant C/G;T snv 8.0E-06; 2.4E-05; 4.0E-06 1
rs772747361 1.000 0.040 4 169585461 missense variant C/A;T snv 2.0E-05 1
rs779770049 1.000 0.040 14 96855230 missense variant T/G snv 8.0E-06 1
rs895824243 1.000 0.040 10 13110387 missense variant A/C snv 1
rs1159805691 0.851 0.080 16 1792266 frameshift variant T/- del 7.0E-06 4
rs121912441 0.925 0.080 21 31667359 missense variant T/C snv 4.8E-05 7.0E-06 2
rs1445888481 0.925 0.080 2 112835572 synonymous variant C/T snv 7.0E-06 2
rs574548474 0.925 0.040 9 131128389 missense variant T/C snv 7.0E-06 2
rs758440592 0.882 0.120 12 53314832 missense variant C/T snv 2.0E-05 7.0E-06 4
rs137852973 0.752 0.200 11 62702493 missense variant G/A;C snv 7.0E-06 13
rs760982722 0.925 0.080 17 44915224 missense variant C/T snv 2.4E-05 1.4E-05 2
rs905184241 1.000 0.040 12 64481858 missense variant C/G snv 1.2E-05 1.4E-05 1
rs745805222 0.790 0.120 12 102475722 synonymous variant C/T snv 1.2E-05 4.9E-05 7
rs776098853 1.000 0.040 4 169508292 missense variant A/T snv 1.0E-04 6.3E-05 1
rs142812715 1.000 0.040 10 13124053 missense variant A/T snv 1.5E-04 7.0E-05 1
rs28942073 0.851 0.120 5 74718804 missense variant C/T snv 5.9E-04 4.5E-04 4
rs80265967 0.732 0.200 21 31667290 missense variant A/C;T snv 1.4E-03 1.2E-03 16
rs34324114 1.000 0.040 4 169477323 missense variant A/C snv 4.6E-03 4.1E-03 1
rs1138272 0.611 0.600 11 67586108 missense variant C/T snv 5.9E-02 5.5E-02 42