Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs771563543 0.851 0.040 10 31510841 missense variant G/A snv 4.0E-06 1.4E-05 5
rs745564626 0.752 0.280 14 103699003 missense variant C/G;T snv 4.3E-05 14
rs25487 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs25489 0.550 0.720 19 43552260 missense variant C/G;T snv 8.5E-06; 7.1E-02 78
rs1476157710 0.925 0.040 12 48970460 missense variant T/C snv 4.1E-06 1.4E-05 3
rs774265827 6 43780773 missense variant G/A;T snv 8.0E-06; 2.0E-05 1
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
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
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