Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1799983 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs4986790 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs77375493 0.458 0.760 9 5073770 missense variant G/A;T snv 3.5E-04 187
rs1800470 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 107
rs1267969615
ACE
0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 100
rs1544410
VDR
0.542 0.760 12 47846052 intron variant C/A;G;T snv 78
rs1800471 0.597 0.840 19 41352971 missense variant C/G;T snv 5.6E-02 48
rs2292832 0.605 0.640 2 240456086 non coding transcript exon variant T/A;C snv 0.59 46
rs28929474 0.708 0.320 14 94378610 missense variant C/G;T snv 2.8E-05; 1.1E-02 37
rs28934571 0.645 0.360 17 7674216 missense variant C/A;G snv 31
rs1127354 0.667 0.400 20 3213196 missense variant C/A;G snv 7.5E-02 26
rs1275561861 0.672 0.360 6 29944350 missense variant G/A snv 23
rs641738 0.689 0.320 19 54173068 missense variant T/A;C;G snv 22
rs2287622 0.724 0.240 2 168973818 missense variant A/C;G;T snv 0.57 16
rs72613567 0.742 0.320 4 87310240 splice donor variant -/A delins 0.22 14
rs236918 0.776 0.160 11 117220893 non coding transcript exon variant G/A;C snv 10
rs1161457931 0.763 0.200 22 37084836 missense variant C/T snv 6.4E-06 9
rs10053538 0.807 0.160 5 157110499 intron variant C/A;T snv 7
rs57749775 0.851 0.080 12 52904822 missense variant A/G;T snv 1.7E-03; 4.0E-06 6
rs1054690270 0.827 0.160 8 144505907 frameshift variant CT/- delins 5
rs5743314 0.851 0.160 4 186079221 intron variant G/C;T snv 5
rs10433937 0.882 0.080 4 87308948 intron variant T/A;C;G snv 4
rs1346044973 0.851 0.160 5 1294158 missense variant G/A snv 1.1E-05 4
rs4656942 0.851 0.160 1 160861258 intron variant G/A;C;T snv 4
rs137853590 0.882 0.160 16 30751140 stop gained C/T snv 4.0E-06 3