Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs135745 0.763 0.200 22 38287631 downstream gene variant G/C snv 0.48 13
rs112538845 0.925 0.040 4 184084475 downstream gene variant C/T snv 1.7E-02 3
rs201921722 0.925 0.040 11 123679999 downstream gene variant -/A delins 9.2E-06 3
rs2137947 0.882 0.040 3 4989276 downstream gene variant C/T snv 0.64 3
rs34102224 0.925 0.040 8 5364506 downstream gene variant G/C snv 0.12 3
rs25531 0.581 0.520 17 30237328 upstream gene variant T/C snv 0.18 72
rs1800587 0.620 0.720 2 112785383 upstream gene variant G/A;C snv 0.32 43
rs6311 0.645 0.640 13 46897343 upstream gene variant C/T snv 0.40 41
rs4570625 0.724 0.200 12 71938143 upstream gene variant G/T snv 0.27 25
rs334558 0.701 0.320 3 120094435 upstream gene variant A/G snv 0.51 20
rs4291
ACE
0.724 0.400 17 63476833 upstream gene variant T/A;C snv 20
rs11178997 0.827 0.040 12 71938373 upstream gene variant T/A snv 0.12 5
rs945032 0.882 0.040 14 96204324 upstream gene variant T/C snv 0.78 5
rs10447760 0.851 0.040 7 114083210 upstream gene variant C/T snv 0.17 4
rs111365677 0.925 0.040 1 99463578 upstream gene variant T/C snv 2.3E-03 3
rs182377406 0.925 0.040 11 67449378 upstream gene variant A/G snv 4.5E-04 3
rs55679149 0.925 0.040 1 89068655 upstream gene variant C/T snv 0.34 3
rs2551941 0.925 0.040 2 207627419 upstream gene variant A/G;T snv 2
rs4810896 0.925 0.040 20 48918761 upstream gene variant A/C;G snv 2
rs2228570
VDR
0.521 0.760 12 47879112 start lost A/C;G;T snv 0.63 99
rs2302045 0.851 0.040 2 241081801 splice region variant G/A snv 7.6E-02 1.0E-01 4
rs165599 0.677 0.280 22 19969258 3 prime UTR variant G/A snv 0.56 27
rs806368 0.752 0.280 6 88140381 3 prime UTR variant T/C snv 0.19 14
rs3746544 0.790 0.120 20 10306436 3 prime UTR variant G/T snv 0.68 10
rs7124442 0.827 0.160 11 27655494 3 prime UTR variant C/G;T snv 9