Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1042522 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs1131691014 0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs878854066 0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs28934576 0.554 0.600 17 7673802 missense variant C/A;G;T snv 4.0E-06; 1.6E-05 78
rs11540652 0.592 0.640 17 7674220 missense variant C/A;G;T snv 1.2E-05 57
rs762846821 0.614 0.320 17 7675151 missense variant C/A;T snv 8.0E-06 57
rs121912651 0.605 0.680 17 7674221 missense variant G/A;C snv 4.0E-06 53
rs28934578 0.605 0.600 17 7675088 missense variant C/A;T snv 4.0E-06 47
rs121912664 0.630 0.320 17 7670699 missense variant C/A;G;T snv 1.2E-05 44
rs121913343 0.611 0.520 17 7673803 missense variant G/A;C;T snv 1.2E-05 44
rs55819519 0.627 0.400 17 7673751 missense variant C/A;G;T snv 1.6E-04 1.3E-04 40
rs28934575 0.641 0.400 17 7674230 missense variant C/A;G;T snv 37
rs78378222 0.662 0.360 17 7668434 3 prime UTR variant T/G snv 8.3E-03 37
rs1057519975 0.649 0.480 17 7675209 missense variant A/C;G;T snv 34
rs121912666 0.645 0.360 17 7674872 missense variant T/C;G snv 8.0E-06 34
rs397516436 0.641 0.440 17 7674894 stop gained G/A;C snv 34
rs760043106 0.645 0.440 17 7674947 missense variant A/C;G;T snv 32
rs886039484 0.641 0.440 17 7674888 missense variant T/C;G snv 32
rs28934571 0.645 0.360 17 7674216 missense variant C/A;G snv 31
rs28934574 0.658 0.440 17 7673776 missense variant G/A;C snv 4.0E-06 31
rs587778720 0.667 0.360 17 7674893 missense variant C/A;G;T snv 4.0E-06 31
rs121912656 0.662 0.560 17 7674229 missense variant C/A;G;T snv 4.0E-06; 4.0E-06 28
rs28934573 0.667 0.480 17 7674241 missense variant G/A;C;T snv 4.0E-06 28
rs879253942 0.677 0.400 17 7673826 missense variant A/G snv 28
rs1057519991 0.662 0.440 17 7675076 missense variant T/A;C;G snv 4.0E-06 26