Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs759834365 0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs953038635 0.590 0.800 6 159692720 missense variant G/A;T snv 8.0E-06 51
rs6318 0.623 0.520 X 114731326 missense variant C/G;T snv 42
rs995922697 0.724 0.560 3 49357413 missense variant A/G snv 4.1E-06 15
rs3730358 0.724 0.360 14 104780070 intron variant G/A;C snv 0.16; 4.0E-03 14
rs10828317 0.776 0.280 10 22550699 missense variant T/C snv 9
rs781598341 0.827 0.240 6 159682510 missense variant T/C snv 4.0E-06 5
rs1182593032 0.851 0.200 16 69718516 missense variant A/G snv 4
rs1231813088 0.851 0.160 10 92690015 missense variant C/T snv 4
rs1322425552 0.851 0.160 17 74923048 missense variant G/A snv 4
rs1457049406 0.851 0.200 22 19962555 missense variant C/T snv 4
rs6805251 0.925 0.120 3 119841759 intron variant T/A;C snv 4
rs1402139464 0.882 0.160 11 27701009 5 prime UTR variant G/A;T snv 8.4E-06 3
rs1447119000 0.925 0.120 22 42130763 missense variant G/A snv 2
rs1890196 0.925 0.120 1 66337397 intron variant C/G;T snv 2
rs2445142 0.925 0.120 1 21899250 intron variant G/A;C snv 2
rs2701124 0.925 0.120 12 52054373 synonymous variant G/A;C snv 9.5E-02 2
rs6587002 0.925 0.120 8 21723708 intron variant T/C;G snv 2
rs767413934 0.925 0.120 11 113424539 missense variant G/A snv 4.0E-06 2
rs905568 0.925 0.120 3 114232449 non coding transcript exon variant C/A;G;T snv 2
rs1258159645 0.630 0.600 16 69711128 missense variant G/A snv 7.0E-06 37
rs1322643228 0.807 0.280 12 104321110 missense variant C/T snv 7.1E-06 6
rs1330075052 0.882 0.160 12 104215828 missense variant T/C snv 1.4E-05 3
rs76980269 0.763 0.280 12 117330794 synonymous variant G/A snv 2.8E-05 4.2E-05 10
rs201934979 0.882 0.160 15 74749838 missense variant C/T snv 8.8E-05; 8.0E-06 1.3E-04 3