Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1020608562 0.807 0.160 3 46373738 missense variant T/C snv 4.0E-06 9
rs1044498 0.752 0.360 6 131851228 missense variant A/C;G snv 0.19 15
rs1045642 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs10887800 0.790 0.280 10 88316086 intron variant A/G;T snv 11
rs10951982 0.851 0.160 7 6382925 intron variant G/A;T snv 5
rs1162592300
ALB
0.925 0.080 4 73412045 missense variant G/A snv 3
rs1188383936
F2
0.524 0.760 11 46725976 missense variant C/T snv 8.0E-06 102
rs12137135 0.925 0.080 1 22348728 intergenic variant A/C;G snv 2
rs121908529 0.851 0.160 2 240871433 missense variant G/A;C snv 5.6E-04 4
rs1222213359 0.574 0.720 6 43770966 missense variant G/A snv 62
rs1232898090 0.637 0.600 22 46198429 missense variant G/C;T snv 4.0E-06; 4.0E-06 40
rs12513649 0.851 0.160 5 173045049 regulatory region variant C/G;T snv 6
rs1267969615
ACE
0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 100
rs13447075 0.882 0.120 8 127998344 non coding transcript exon variant C/A snv 4
rs1372834938 0.763 0.280 2 8812465 missense variant G/C snv 4.2E-06 12
rs145640112 0.925 0.080 4 186250267 missense variant A/C;G snv 1.8E-04; 4.0E-06 2
rs1516792 0.925 0.080 2 112778356 intron variant G/A snv 2
rs1544410
VDR
0.542 0.760 12 47846052 intron variant C/A;G;T snv 78
rs161740 0.882 0.200 5 98869326 intron variant C/A;T snv 3
rs1617640
EPO
0.742 0.520 7 100719675 upstream gene variant C/A;G;T snv 15
rs17089362 0.882 0.160 18 74518403 non coding transcript exon variant G/A;T snv 3
rs17817449
FTO
0.716 0.560 16 53779455 intron variant T/A;G snv 21
rs1799983 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs1800470 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 107
rs1801239 0.827 0.160 10 16877053 missense variant T/C;G snv 8.9E-02; 8.0E-06 8