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
rs12951053 0.732 0.160 17 7674089 intron variant A/C snv 0.10 14
rs7248488 0.851 0.160 19 22005907 intron variant A/C snv 0.59 5
rs7763881 0.776 0.160 6 8653014 non coding transcript exon variant A/C snv 0.44 11
rs8103163 0.882 0.120 19 21991950 intron variant A/C snv 0.59 4
rs1131691021 0.716 0.120 17 7675097 missense variant A/C;G snv 21
rs1989969
VDR
0.827 0.120 12 47884227 intron variant A/C;G;T snv 0.60 8
rs2228570
VDR
0.521 0.760 12 47879112 start lost A/C;G;T snv 0.63 99
rs2273535 0.645 0.360 20 56386485 missense variant A/C;T snv 0.28 38
rs6505162 0.695 0.320 17 30117165 5 prime UTR variant A/C;T snv 0.50; 3.1E-05 25
rs10509670 0.851 0.080 10 94308190 intron variant A/G snv 0.30 5
rs11615 0.572 0.640 19 45420395 synonymous variant A/G snv 0.50 0.55 62
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs13016963 0.851 0.080 2 201298088 intron variant A/G snv 0.59 5
rs16944 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 92
rs1695 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs1800682 0.637 0.440 10 88990206 non coding transcript exon variant A/G snv 0.54 32
rs1800871 0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 108
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 135
rs181206 0.742 0.440 16 28502082 missense variant A/G snv 0.28 0.24 16
rs2072472 0.732 0.200 2 102026557 intron variant A/G snv 0.24 13
rs2274223 0.620 0.400 10 94306584 missense variant A/G snv 0.28 0.31 40
rs2308321 0.653 0.480 10 129766800 missense variant A/G snv 9.3E-02 8.7E-02 29
rs2320615 0.925 0.080 4 163148797 intron variant A/G snv 0.78 3
rs3746444 0.514 0.760 20 34990448 mature miRNA variant A/G snv 0.20 0.19 105