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
rs1045642 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs1131691014 0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs121912656 0.662 0.560 17 7674229 missense variant C/A;G;T snv 4.0E-06; 4.0E-06 28
rs1800470 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 107
rs1800925 0.627 0.560 5 132657117 non coding transcript exon variant C/G;T snv 37
rs397516436 0.641 0.440 17 7674894 stop gained G/A;C snv 34
rs4644 0.732 0.320 14 55138217 missense variant C/A;G snv 0.35 14
rs878854066 0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1136410 0.559 0.760 1 226367601 missense variant A/G snv 0.21 0.15 70
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 135
rs1801133 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
rs1801275 0.581 0.680 16 27363079 missense variant A/G snv 0.25 0.36 58
rs5498 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 99
rs2010963 0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68 82
rs1800871 0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 108
rs25487 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205