Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1131691014 0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs1057519981 0.689 0.440 17 7674251 missense variant A/C;G;T snv 22
rs113488022 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs760043106 0.645 0.440 17 7674947 missense variant A/C;G;T snv 32
rs876660821 0.689 0.400 17 7675075 missense variant A/C;G;T snv 22
rs1057519983 0.724 0.360 17 7673797 missense variant A/G snv 16
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs104894226 0.658 0.560 11 534285 missense variant C/A;G;T snv 29
rs104894228 0.605 0.560 11 534286 missense variant C/A;G;T snv 48
rs1057519895 0.724 0.240 4 152328232 missense variant C/A;G;T snv 17
rs11540652 0.592 0.640 17 7674220 missense variant C/A;G;T snv 1.2E-05 57
rs121912655 0.724 0.400 17 7674238 missense variant C/A;G;T snv 15
rs28934576 0.554 0.600 17 7673802 missense variant C/A;G;T snv 4.0E-06; 1.6E-05 78
rs730882005 0.701 0.400 17 7674250 missense variant C/A;G;T snv 8.0E-06 20
rs764146326 0.662 0.480 17 7673779 missense variant C/A;G;T snv 4.0E-06 25
rs863224451 0.701 0.440 17 7673796 missense variant C/A;G;T snv 20
rs1057519896 0.742 0.320 4 152326136 missense variant C/A;T snv 12
rs193920774 0.695 0.440 17 7673823 missense variant C/A;T snv 22
rs397516896 0.763 0.360 7 140753355 missense variant C/G;T snv 11
rs11614913 0.512 0.760 12 53991815 mature miRNA variant C/T snv 0.39 0.34 111
rs5443 0.532 0.760 12 6845711 synonymous variant C/T snv 0.36 0.44 106
rs1799782 0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02 151
rs121912651 0.605 0.680 17 7674221 missense variant G/A;C snv 4.0E-06 53
rs138729528 0.677 0.480 17 7675089 missense variant G/A;C snv 1.6E-05 25
rs375874539 0.732 0.320 17 7674237 missense variant G/A;C snv 15