Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10069690 0.595 0.560 5 1279675 intron variant C/T snv 0.36 53
rs55705857 0.732 0.080 8 129633446 intron variant A/G snv 3.9E-02 16
rs7003908 0.716 0.320 8 47858141 intron variant C/A snv 0.66 16
rs11571833 0.608 0.360 13 32398489 stop gained A/T snv 6.6E-03 6.0E-03 43
rs13181 0.487 0.760 19 45351661 stop gained T/A;G snv 4.0E-06; 0.32 134
rs1042522 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs1136410 0.559 0.760 1 226367601 missense variant A/G snv 0.21 0.15 70
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs121913286 0.677 0.280 3 179218306 missense variant C/A;G snv 23
rs121913500 0.529 0.600 2 208248388 missense variant C/A;G;T snv 4.0E-06 96
rs1695 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs1800470 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 107
rs1801133 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 135
rs25487 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs28934576 0.554 0.600 17 7673802 missense variant C/A;G;T snv 4.0E-06; 1.6E-05 78
rs4644 0.732 0.320 14 55138217 missense variant C/A;G snv 0.35 14
rs5498 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 99
rs861539 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 104
rs878854066 0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs2736098 0.600 0.600 5 1293971 synonymous variant C/T snv 0.29 0.22 48
rs758272654 0.611 0.680 20 58909201 synonymous variant T/C snv 4.0E-06 7.0E-06 50
rs1800871 0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 108
rs1801320 0.742 0.160 15 40695330 5 prime UTR variant G/C snv 0.12 15
rs2010963 0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68 82