Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1023835002 0.763 0.280 15 44711547 start lost A/G;T snv 10
rs1042522 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
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
rs104894229 0.564 0.600 11 534289 missense variant C/A;G;T snv 73
rs104894230 0.564 0.600 11 534288 missense variant C/A;G;T snv 73
rs1056836 0.581 0.680 2 38071060 missense variant G/C snv 0.51 58
rs1057519877 0.763 0.280 15 44711549 start lost G/A snv 10
rs1057519879 0.763 0.280 15 44711548 start lost T/C;G snv 10
rs1057519933 0.790 0.240 3 179199156 missense variant A/G snv 11
rs1057519934 0.790 0.240 3 179199158 missense variant G/C snv 11
rs1057519935 0.790 0.240 3 179199157 missense variant A/G snv 11
rs1057519977 0.763 0.360 17 7675189 missense variant G/C snv 13
rs1057519978 0.763 0.360 17 7675191 missense variant A/C;G;T snv 12
rs1057519981 0.689 0.440 17 7674251 missense variant A/C;G;T snv 22
rs1057519983 0.724 0.360 17 7673797 missense variant A/G snv 16
rs1057519996 0.701 0.360 17 7675217 splice acceptor variant T/A;C;G snv 19
rs1057520007 0.701 0.440 17 7674917 missense variant T/A;C;G snv 21
rs113488022 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs11540652 0.592 0.640 17 7674220 missense variant C/A;G;T snv 1.2E-05 57
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs121912651 0.605 0.680 17 7674221 missense variant G/A;C snv 4.0E-06 53
rs121912657 0.683 0.480 17 7673806 missense variant C/A;G;T snv 4.0E-06 24
rs121913233 0.627 0.520 11 533874 missense variant T/A;C;G snv 37
rs121913338 0.677 0.400 7 140753354 missense variant T/A;C;G snv 24