Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs146052672 0.851 0.160 6 34242693 intron variant -/C delins 5
rs12500426 0.851 0.240 4 94593458 intron variant A/C snv 0.54 5
rs1372503923 0.925 0.160 5 53048731 missense variant A/C snv 3
rs201739205 0.851 0.200 17 42552898 5 prime UTR variant A/C snv 7.8E-03 8.2E-03 5
rs316019 0.790 0.360 6 160249250 missense variant A/C snv 0.90 0.89 8
rs35036378 0.851 0.200 14 64294403 5 prime UTR variant A/C snv 7.0E-03 5
rs5186 0.630 0.560 3 148742201 3 prime UTR variant A/C snv 0.23 0.21 38
rs1043307 0.776 0.360 12 121915890 missense variant A/C;G snv 14
rs2228570
VDR
0.521 0.760 12 47879112 start lost A/C;G;T snv 0.63 99
rs35767 0.763 0.360 12 102481791 upstream gene variant A/C;G;T snv 13
rs7310409 0.925 0.160 12 120987058 intron variant A/C;G;T snv 7
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
rs1004467 0.790 0.280 10 102834750 non coding transcript exon variant A/G snv 0.15 0.14 13
rs10224002 0.925 0.080 7 151717955 intron variant A/G snv 0.31 12
rs10741657 0.637 0.520 11 14893332 upstream gene variant A/G snv 0.65 34
rs10757274 0.701 0.320 9 22096056 intron variant A/G snv 0.41 22
rs10757278 0.620 0.520 9 22124478 intron variant A/G snv 0.40 44
rs10938397 0.851 0.200 4 45180510 intergenic variant A/G snv 0.37 19
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
rs13333226 0.827 0.200 16 20354332 intron variant A/G snv 0.23 10
rs16944 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 92