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
rs854560 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 113
rs17465637 0.790 0.200 1 222650187 intron variant A/C;G;T snv 0.64; 6.4E-06 11
rs2228570
VDR
0.521 0.760 12 47879112 start lost A/C;G;T snv 0.63 99
rs2228145 0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 57
rs699947 0.570 0.680 6 43768652 upstream gene variant A/C;T snv 67
rs1024611 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 63
rs10903323 0.807 0.160 8 10292057 intron variant A/G snv 0.15 8
rs11066301 0.827 0.200 12 112433568 intron variant A/G snv 0.30 12
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
rs1570360 0.641 0.680 6 43770093 upstream gene variant A/G snv 0.76 38
rs1800469 0.547 0.760 19 41354391 intron variant A/G snv 0.69 78
rs1800625 0.641 0.680 6 32184665 upstream gene variant A/G snv 0.15 39
rs1800871 0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 108
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
rs2071559
KDR
0.667 0.680 4 55126199 upstream gene variant A/G snv 0.53 26
rs2072633 0.807 0.320 6 31951801 3 prime UTR variant A/G snv 0.59 6
rs3746444 0.514 0.760 20 34990448 mature miRNA variant A/G snv 0.20 0.19 105
rs3811047 0.807 0.400 2 112913833 missense variant A/G snv 0.71 0.60 10
rs3819024 0.701 0.560 6 52185988 upstream gene variant A/G snv 0.34 17
rs4420638 0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 43
rs4711998 0.708 0.360 6 52185555 upstream gene variant A/G snv 0.64 16
rs5498 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 99