Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10025419 4 100647799 intron variant G/A snv 0.87 1
rs10041590 5 24064827 intron variant T/C;G snv 2
rs10054178 5 24059742 intron variant A/G snv 7.5E-02 2
rs10056373 5 24069684 intron variant C/T snv 7.4E-02 2
rs10119043 9 135122706 downstream gene variant C/T snv 0.11 2
rs1015164 0.925 3 46410189 intron variant A/C;G;T snv 8
rs10178992 2 233749231 intron variant T/A snv 0.37 4
rs10179091 2 233749337 intron variant T/C snv 0.49 4
rs1042522 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs10484554 0.807 0.200 6 31306778 intron variant C/T snv 0.12 11
rs10827209 10 33198261 intron variant A/C snv 0.23 2
rs10892961 11 123093392 intron variant A/C;G;T snv 2
rs10929301 2 233755003 splice region variant C/G;T snv 0.48 4
rs10929302 2 233757136 intron variant G/A snv 0.30 4
rs11011237 10 37531016 intron variant G/A snv 9.2E-02 2
rs11012476 0.925 0.120 10 21003994 intron variant C/T snv 3.5E-02 3
rs11087114 20 14931037 intron variant G/A;C snv 1
rs11218976 11 123090950 intron variant A/G snv 0.41 2
rs11228672 11 56597931 non coding transcript exon variant G/A;C snv 2
rs113051092 5 24060490 intron variant A/T snv 7.4E-02 2
rs113162402 17 58522103 splice acceptor variant T/A snv 1
rs1131691014 0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs11568350 0.790 0.240 2 189565370 missense variant C/A snv 3.8E-03 1.6E-02 9
rs11673726 2 233755414 non coding transcript exon variant G/A;T snv 4
rs11695484 2 233745803 intron variant A/G snv 0.30 3