Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1318358361 0.724 0.240 6 156778678 missense variant C/G snv 2.1E-05 13
rs7626962 0.790 0.080 3 38579416 missense variant G/A;T snv 1.6E-05; 5.9E-03 10
rs80356779 0.776 0.320 11 68780662 missense variant G/A snv 3.2E-05 5.6E-05 10
rs199473097 0.763 0.120 3 38606710 missense variant G/A snv 8.0E-06 7.0E-06 9
rs72546668 0.807 0.200 3 8745644 missense variant C/A;T snv 4.0E-06; 2.6E-03 8
rs794728708 0.827 0.120 1 237377386 missense variant G/A;T snv 8
rs2266782 0.851 0.200 1 171107825 missense variant G/A snv 0.37 0.41 7
rs1130183 0.827 0.160 1 160041722 missense variant G/A snv 4.6E-02 4.7E-02 6
rs199473124 0.851 0.120 3 38603902 missense variant A/T snv 8.0E-06 7.0E-06 4
rs199473604 0.882 0.120 3 38560394 missense variant G/T snv 4
rs121434278 0.882 0.120 1 75740094 missense variant G/A snv 4.0E-05 7.0E-05 3
rs137854609 0.882 0.120 3 38581170 missense variant C/A;T snv 7.9E-05 3
rs199473320 0.882 0.120 3 38550878 missense variant G/C snv 6.0E-05 4.0E-04 3
rs77931234 0.925 0.120 1 75761161 missense variant A/C;G snv 3.3E-03 3
rs786205867 0.882 0.080 1 111787039 missense variant C/T snv 3
rs116840776 1.000 0.040 3 8745627 missense variant C/G snv 1.4E-03 1.6E-03 2
rs1188884950 0.925 0.080 5 474952 missense variant A/G snv 4.2E-06 2
rs121909281 0.925 0.120 3 8733916 missense variant G/A;C snv 4.3E-04 2
rs121909282 0.925 0.120 3 8745647 missense variant T/G snv 1.4E-05 2
rs1361625573 0.925 0.080 5 474979 missense variant A/G snv 7.0E-06 2
rs137854610 0.925 0.120 3 38550895 missense variant C/T snv 2.8E-05 1.7E-04 2
rs149344567 0.925 0.120 1 111776247 missense variant C/T snv 6.4E-05 5.6E-05 2
rs199472728 0.925 0.120 11 2572885 missense variant A/G snv 1.8E-04 1.3E-04 2
rs199473014 0.925 0.120 7 150947684 missense variant G/T snv 2.1E-05 2
rs199473573 0.925 0.120 3 38604007 missense variant A/C snv 1.6E-05 7.0E-06 2