Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs1800795 0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs1800896 0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs2071746 0.708 0.320 22 35380679 intron variant A/T snv 0.49 18
rs2075650 0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 45
rs2234693 0.555 0.680 6 151842200 intron variant T/C snv 0.47 77
rs2526378 0.925 0.120 17 58326988 intron variant A/G snv 0.51 2
rs4717806 0.776 0.200 7 73702147 intron variant T/A;C snv 9
rs4769874 0.827 0.240 13 30752304 intron variant G/A snv 5.8E-02 5
rs7044343 0.752 0.520 9 6254208 intron variant C/T snv 0.51 13
rs7396366 0.925 0.120 11 986185 intron variant C/A snv 0.58 2
rs8100239 0.882 0.200 19 44749847 intron variant T/A snv 0.38 5
rs9340799 0.583 0.680 6 151842246 intron variant A/G snv 0.32 62
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs328
LPL
0.732 0.440 8 19962213 stop gained C/G snv 9.2E-02 9.0E-02 19
rs1035071612 0.763 0.240 19 11113361 missense variant C/A;T snv 4.0E-06 9
rs1042522 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs1051338 0.807 0.120 10 89247603 missense variant T/G snv 0.32 0.26 7
rs1052133 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs1061170
CFH
0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 72
rs1065852 0.695 0.360 22 42130692 missense variant G/A snv 0.21 0.19 19
rs1136410 0.559 0.760 1 226367601 missense variant A/G snv 0.21 0.15 70
rs1137101 0.554 0.760 1 65592830 missense variant A/G snv 0.51 0.50 77