Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1024611 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 63
rs2943641 0.763 0.160 2 226229029 intergenic variant T/C snv 0.67 18
rs3093077 0.827 0.200 1 159709846 upstream gene variant A/C;G;T snv 9
rs495828 0.827 0.200 9 133279294 upstream gene variant T/G snv 0.81 24
rs7923837 0.882 0.160 10 92722160 intergenic variant G/A;T snv 8
rs2230806 0.689 0.280 9 104858586 missense variant C/T snv 0.32 0.39 24
rs1045642 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs2231142 0.583 0.680 4 88131171 missense variant G/C;T snv 4.0E-06; 0.12 56
rs505922
ABO
0.689 0.520 9 133273813 intron variant C/T snv 34
rs1267969615
ACE
0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 100
rs266729 0.637 0.560 3 186841685 upstream gene variant C/A;G;T snv 37
rs822395 0.776 0.240 3 186849018 intron variant C/A;G snv 10
rs822396 0.732 0.400 3 186849088 intron variant G/A snv 0.81 16
rs1063538 1.000 0.080 3 186856394 3 prime UTR variant T/C snv 0.55 4
rs1501299 0.597 0.720 3 186853334 intron variant G/C;T snv 52
rs2241766 0.608 0.720 3 186853103 synonymous variant T/C;G snv 8.0E-06; 0.13 48
rs4994 0.578 0.640 8 37966280 missense variant A/G snv 0.11 9.2E-02 65
rs2070600 0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 82
rs1800625 0.641 0.680 6 32184665 upstream gene variant A/G snv 0.15 39
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134
rs671 0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 116
rs1044250 0.807 0.240 19 8371280 missense variant C/T snv 0.30 0.29 12
rs1800497 0.620 0.400 11 113400106 missense variant G/A snv 0.26 0.26 56
rs189037
ATM ; NPAT
0.689 0.400 11 108223106 5 prime UTR variant G/A snv 0.49 22
rs1800469 0.547 0.760 19 41354391 intron variant A/G snv 0.69 78