Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1008805 0.851 0.160 15 51257402 intron variant G/A snv 0.64 7
rs1314386070 0.827 0.240 8 90042766 missense variant T/C snv 1.4E-05 9
rs1333049 0.614 0.520 9 22125504 intron variant G/C snv 0.41 60
rs1544410
VDR
0.542 0.760 12 47846052 intron variant C/A;G;T snv 78
rs1799752
ACE
0.677 0.480 17 63488529 intron variant -/TTTTTTTTTTTGAGACGGAGTCTCGCTCTGTCGCCCATACAGTCACTTTT delins 25
rs1799889 0.649 0.600 7 101126430 upstream gene variant A/G snv 31
rs1800795 0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs1805192 0.510 0.840 3 12379739 missense variant C/G snv 121
rs187238 0.602 0.680 11 112164265 intron variant C/A;G snv 48
rs2016520 0.752 0.320 6 35411001 5 prime UTR variant C/T snv 0.78 16
rs20417 0.576 0.600 1 186681189 non coding transcript exon variant C/G;T snv 57
rs2234693 0.555 0.680 6 151842200 intron variant T/C snv 0.47 77
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs4291
ACE
0.724 0.400 17 63476833 upstream gene variant T/A;C snv 20
rs4420638 0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 43
rs5963409
OTC
1.000 0.080 X 38351716 intron variant A/C;G snv 3
rs6318 0.623 0.520 X 114731326 missense variant C/G;T snv 42
rs899127658
F2
0.547 0.720 11 46739084 missense variant G/A;C snv 82
rs9340799 0.583 0.680 6 151842246 intron variant A/G snv 0.32 62
rs9794 0.882 0.200 6 35428018 3 prime UTR variant G/A;C;T snv 4
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1416580204
MOK
0.608 0.720 14 102250837 missense variant C/T snv 4.0E-06 7.0E-06 49
rs4986790 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193