Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs642961 0.732 0.440 1 209815925 intergenic variant A/G snv 0.84 14
rs135745 0.763 0.200 22 38287631 downstream gene variant G/C snv 0.48 13
rs79767424 0.827 0.080 5 19108581 intron variant G/T snv 4.1E-02 7
rs1800628 0.827 0.080 6 31579073 downstream gene variant G/A snv 7.3E-02 6
rs3129780 0.827 0.080 6 32679924 intergenic variant T/A;C snv 6
rs708111 0.882 0.120 1 228003664 upstream gene variant G/A snv 0.48 4
rs7834169 0.925 0.120 8 27052774 upstream gene variant C/G snv 0.16 3
rs1373756 1.000 0.120 18 52259936 intergenic variant C/T snv 0.24 2
rs221236 1.000 0.120 7 157529938 downstream gene variant G/A snv 0.96 2
rs1799752
ACE
0.677 0.480 17 63488529 intron variant -/TTTTTTTTTTTGAGACGGAGTCTCGCTCTGTCGCCCATACAGTCACTTTT delins 25
rs61573157 0.882 0.160 10 70760503 missense variant C/T snv 8.6E-02 7.5E-02 6
rs1229984 0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 83
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
rs1800870 0.851 0.200 17 19649164 intron variant C/T snv 5
rs1130409 0.555 0.720 14 20456995 missense variant T/A;C;G snv 4.0E-06; 4.0E-06; 0.42 72
rs2071676 0.925 0.120 9 35674056 missense variant G/A snv 0.37 0.30 4
rs189037
ATM ; NPAT
0.689 0.400 11 108223106 5 prime UTR variant G/A snv 0.49 22
rs2273535 0.645 0.360 20 56386485 missense variant A/C;T snv 0.28 38
rs1047972 0.716 0.240 20 56386407 missense variant T/C snv 0.85 0.84 19
rs1473418 1.000 0.080 18 63319316 5 prime UTR variant C/G snv 0.98 2
rs1950252 1.000 0.080 14 23309489 3 prime UTR variant A/G snv 0.93 2
rs8190315
BID
0.851 0.240 22 17743998 missense variant T/C snv 2.4E-02 3.6E-02 5
rs1048638
CA9
0.807 0.160 9 35681125 3 prime UTR variant C/A;G snv 10
rs3829078
CA9
0.851 0.160 9 35679254 missense variant A/G;T snv 8.2E-02 6