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
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
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
rs876660333 0.742 0.360 17 7673805 missense variant A/C;G;T snv 13
rs1057519933 0.790 0.240 3 179199156 missense variant A/G snv 11
rs1057519935 0.790 0.240 3 179199157 missense variant A/G snv 11
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
rs1695 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs1801394 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 101
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 135
rs1023835002 0.763 0.280 15 44711547 start lost A/G;T snv 10
rs866775781 0.716 0.440 17 7675216 splice acceptor variant C/A;G snv 17
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
rs11540652 0.592 0.640 17 7674220 missense variant C/A;G;T snv 1.2E-05 57
rs121912657 0.683 0.480 17 7673806 missense variant C/A;G;T snv 4.0E-06 24
rs121913351 0.776 0.240 7 140781611 missense variant C/A;G;T snv 4.0E-06 9
rs28934576 0.554 0.600 17 7673802 missense variant C/A;G;T snv 4.0E-06; 1.6E-05 78
rs483352697 0.695 0.480 17 7674944 missense variant C/A;G;T snv 4.0E-06 21
rs730882005 0.701 0.400 17 7674250 missense variant C/A;G;T snv 8.0E-06 20