Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12611084 0.925 0.080 19 38255632 intron variant A/C;G;T snv 2
rs699947 0.570 0.680 6 43768652 upstream gene variant A/C;T snv 67
rs7041
GC
0.576 0.800 4 71752617 missense variant A/C;T snv 0.52; 4.0E-06 64
rs2273535 0.645 0.360 20 56386485 missense variant A/C;T snv 0.28 38
rs1447295 0.658 0.400 8 127472793 intron variant A/C;T snv 29
rs1057519966 0.882 0.080 17 49619064 missense variant A/C;T snv 3
rs4955720 0.925 0.080 3 170310812 downstream gene variant A/C;T snv 2
rs5945372 0.925 0.080 X 153400456 intron variant A/C;T snv 2
rs7611694 0.925 0.080 3 113556777 intron variant A/C;T snv 2
rs142463603 1.000 0.080 8 23649749 intergenic variant A/C;T snv 1
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
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 135
rs4880 0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs1800871 0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 108
rs3746444 0.514 0.760 20 34990448 mature miRNA variant A/G snv 0.20 0.19 105
rs1801394 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 101
rs5498 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 99
rs16944 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 92
rs731236
VDR
0.542 0.760 12 47844974 synonymous variant A/G snv 0.33 0.34 81
rs1137101 0.554 0.760 1 65592830 missense variant A/G snv 0.51 0.50 77
rs17576 0.557 0.760 20 46011586 missense variant A/G snv 0.39 0.36 73
rs1136410 0.559 0.760 1 226367601 missense variant A/G snv 0.21 0.15 70
rs1024611 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 63
rs9340799 0.583 0.680 6 151842246 intron variant A/G snv 0.32 62