Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs200764640 0.925 0.080 7 99666641 missense variant T/C snv 4.0E-06 2
rs1190999960 0.807 0.240 11 65571690 missense variant G/A snv 9
rs1429688220 1.000 0.080 16 31064264 missense variant C/A;T snv 8.0E-06; 4.0E-06 1
rs148738674 1.000 0.080 16 31061261 missense variant C/G;T snv 2.0E-04; 1.0E-05 1
rs553159663 1.000 0.080 16 31062072 missense variant C/T snv 4.0E-06 1
rs8113308 0.925 0.080 19 51942133 intron variant T/C snv 0.24 2
rs1349967796 1.000 0.080 19 37414398 missense variant T/C snv 1.4E-05 1
rs771503724 1.000 0.080 18 58934551 missense variant C/T snv 1.6E-05 1
rs3810151 0.925 0.080 19 42224684 missense variant T/C snv 0.11 7.7E-02 2
rs755035378 1.000 0.080 19 52034210 missense variant C/T snv 8.0E-06 1
rs9940645 0.925 0.080 16 49797677 intron variant A/G snv 0.54 2
rs10235235 0.925 0.080 7 99478208 intron variant T/C snv 0.13 4
rs16917302 0.851 0.080 10 62501439 intron variant A/C snv 0.18 5
rs10822013 0.851 0.080 10 62492218 intron variant C/T snv 0.42 4
rs10995190 0.882 0.080 10 62518923 intron variant G/A snv 0.16 4
rs10995189 1.000 0.080 10 62518422 intron variant G/A snv 0.16 1
rs10995191 1.000 0.080 10 62519115 intron variant C/T snv 0.15 1
rs10995194 1.000 0.080 10 62528371 intron variant G/C snv 0.14 1
rs10995195 1.000 0.080 10 62528630 intron variant T/C snv 0.18 1
rs4746419 1.000 0.080 10 62515502 intron variant C/G snv 0.15 1
rs4986771 0.925 0.080 19 51965039 missense variant A/G snv 3.1E-02 2.7E-02 2
rs2278415 0.925 0.080 19 51964950 missense variant T/A snv 0.16 0.14 2
rs2278420 0.925 0.080 19 51968619 missense variant A/G snv 0.20 0.24 2
rs8109631 0.882 0.080 19 53576890 synonymous variant A/G snv 0.70 0.76 3
rs141660717 1.000 0.080 6 43354899 missense variant T/C snv 7.2E-05 3.6E-04 1