Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1012477 0.827 0.160 1 7798075 intron variant G/C snv 0.16 8
rs1061622 0.633 0.760 1 12192898 missense variant T/G snv 0.22 0.22 33
rs1061624 0.776 0.320 1 12207208 3 prime UTR variant A/G snv 0.48 8
rs1136410 0.559 0.760 1 226367601 missense variant A/G snv 0.21 0.15 70
rs1137100 0.627 0.640 1 65570758 missense variant A/G snv 0.30 0.25 39
rs1137101 0.554 0.760 1 65592830 missense variant A/G snv 0.51 0.50 77
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1537514 0.882 0.120 1 11788011 missense variant G/C snv 0.10 0.10 4
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
rs3219489 0.672 0.360 1 45331833 missense variant C/A;G snv 0.29 0.27 24
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs4645981 0.790 0.160 1 15524988 intron variant G/A;C snv 11
rs5275 0.583 0.560 1 186673926 3 prime UTR variant A/G;T snv 55
rs689466 0.637 0.640 1 186681619 upstream gene variant T/C snv 0.17 33
rs768623239 0.662 0.640 1 109689278 missense variant A/G snv 1.5E-05 26
rs9651118 0.683 0.480 1 11802157 intron variant T/C snv 0.18 20
rs10012 0.716 0.280 2 38075247 missense variant G/C snv 0.31 0.36 16
rs10165970 0.708 0.320 2 100840527 intron variant G/A snv 0.16 18
rs1126497 0.716 0.200 2 47373967 missense variant T/C snv 0.51 0.58 14
rs1143623 0.677 0.440 2 112838252 upstream gene variant C/G snv 0.24 29
rs1143627 0.605 0.760 2 112836810 5 prime UTR variant G/A snv 0.56 47
rs1143634 0.597 0.680 2 112832813 synonymous variant G/A snv 0.19 0.19 52
rs121913500 0.529 0.600 2 208248388 missense variant C/A;G;T snv 4.0E-06 96
rs16944 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 92