Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs751763046 0.790 0.200 1 241885375 missense variant T/C snv 4.0E-06 8
rs763110 0.653 0.560 1 172658358 upstream gene variant C/T snv 0.49 30
rs851797 0.752 0.240 1 241889740 3 prime UTR variant A/G snv 0.72 13
rs9350 0.742 0.240 1 241885372 missense variant C/T snv 0.21 0.19 16
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
rs1056827 0.683 0.400 2 38075034 missense variant C/A snv 0.32 0.35 24
rs1056836 0.581 0.680 2 38071060 missense variant G/C snv 0.51 58
rs1143623 0.677 0.440 2 112838252 upstream gene variant C/G snv 0.24 29
rs1143634 0.597 0.680 2 112832813 synonymous variant G/A snv 0.19 0.19 52
rs1204382931 0.790 0.160 2 38075270 missense variant A/C snv 4.3E-06 10
rs1682111 0.742 0.240 2 54200842 intron variant A/T snv 0.56 13
rs16944 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 92
rs17561 0.672 0.560 2 112779646 missense variant C/A snv 0.27 0.26 23
rs1800440 0.653 0.440 2 38070996 missense variant T/C;G snv 0.15; 4.0E-06 29
rs2292832 0.605 0.640 2 240456086 non coding transcript exon variant T/A;C snv 0.59 46
rs2303425 0.790 0.120 2 47403074 5 prime UTR variant T/C snv 0.10 8
rs3834129 0.627 0.560 2 201232809 upstream gene variant AGTAAG/- del 0.48 38
rs6721961 0.672 0.520 2 177265309 intron variant T/C;G snv 0.89 24
rs104886003 0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 71
rs1050450 0.623 0.600 3 49357401 missense variant G/A snv 0.28 0.30 43
rs1052133 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs121913279 0.526 0.560 3 179234297 missense variant A/G;T snv 4.0E-06; 4.0E-06 101