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 213
rs3783553 0.667 0.480 2 112774138 3 prime UTR variant -/TGAA delins 26
rs61764370 0.662 0.320 12 25207290 3 prime UTR variant A/C snv 6.2E-02 29
rs854560 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 110
rs113488022 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 484
rs1799977 0.662 0.440 3 37012077 missense variant A/C;G;T snv 0.23 28
rs2032582 0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 97
rs2273535 0.645 0.360 20 56386485 missense variant A/C;T snv 0.28 37
rs10505477 0.658 0.400 8 127395198 intron variant A/G snv 0.40 19
rs1128503 0.564 0.760 7 87550285 synonymous variant A/G snv 0.54 0.63 64
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 0.36 187
rs5498 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 97
rs731236
VDR
0.542 0.760 12 47844974 synonymous variant A/G snv 0.33 0.34 81
rs876658657 0.677 0.280 3 37020356 missense variant A/G snv 4.0E-06 24
rs1045642 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs1136201 0.645 0.280 17 39723335 missense variant A/G;T snv 0.20 33
rs121913279 0.526 0.560 3 179234297 missense variant A/G;T snv 4.0E-06; 4.0E-06 62
rs156697 0.672 0.560 10 104279427 missense variant A/G;T snv 0.35 25
rs5275 0.583 0.560 1 186673926 3 prime UTR variant A/G;T snv 55
rs3834129 0.627 0.560 2 201232809 upstream gene variant AGTAAG/- del 0.48 38
rs7958904 0.724 0.200 12 53963768 non coding transcript exon variant C/A;G snv 15
rs121434596 0.677 0.440 1 114716123 missense variant C/A;G;T snv 4.0E-06; 4.0E-06 14
rs121913529 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 135
rs3212986 0.620 0.400 19 45409478 stop gained C/A;G;T snv 0.29; 4.3E-06; 4.3E-06 42