Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs759834365 0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs1045642 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs2228570
VDR
0.521 0.760 12 47879112 start lost A/C;G;T snv 0.63 99
rs2032582 0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 97
rs53576 0.641 0.320 3 8762685 intron variant A/G;T snv 42
rs16139 0.658 0.560 7 24285260 missense variant T/A;C snv 4.0E-06; 3.0E-02 36
rs746682028 0.645 0.480 11 27658414 missense variant C/A;T snv 4.0E-06; 4.0E-06 36
rs1360780 0.708 0.320 6 35639794 intron variant T/A;C snv 31
rs1799752
ACE
0.677 0.480 17 63488529 intron variant -/TTTTTTTTTTTGAGACGGAGTCTCGCTCTGTCGCCCATACAGTCACTTTT delins 25
rs1344706 0.701 0.160 2 184913701 intron variant A/C;T snv 21
rs4291
ACE
0.724 0.400 17 63476833 upstream gene variant T/A;C snv 20
rs5569 0.742 0.280 16 55697923 synonymous variant G/A;C snv 0.31; 4.0E-06 19
rs2710102 0.790 0.120 7 147877298 intron variant A/G;T snv 12
rs4713916 0.790 0.160 6 35702206 intron variant A/C;G;T snv 11
rs1137070 0.763 0.160 X 43744144 synonymous variant T/C snv 0.62 9
rs208294 0.790 0.320 12 121162450 missense variant T/A;C;G snv 0.51 9
rs2242446 0.776 0.080 16 55656513 5 prime UTR variant C/A;T snv 9
rs7124442 0.827 0.160 11 27655494 3 prime UTR variant C/G;T snv 9
rs130058 0.790 0.120 6 77463564 5 prime UTR variant T/A;G snv 8
rs7305115 0.807 0.200 12 71979082 synonymous variant A/C;G;T snv 4.0E-06; 0.56 8
rs1415088003
ACE
0.827 0.160 17 63489038 synonymous variant C/T snv 4.0E-06 7
rs3760138 0.807 0.160 17 76467027 intron variant G/A;T snv 6
rs6195 0.807 0.120 5 143399752 missense variant T/A;C snv 6
rs8150 0.807 0.160 17 76470935 3 prime UTR variant G/A;C snv 6