Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs113488022 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs121913377 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
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
rs762846821 0.614 0.320 17 7675151 missense variant C/A;T snv 8.0E-06 57
rs17655 0.597 0.560 13 102875652 missense variant G/C snv 0.28 0.30 52
rs121913499 0.605 0.520 2 208248389 missense variant G/A;C;T snv 51
rs397517132 0.623 0.280 7 55191846 missense variant A/T snv 48
rs1057519975 0.649 0.480 17 7675209 missense variant A/C;G;T snv 34
rs1057519747 0.716 0.280 17 7675094 missense variant A/C;G;T snv 23