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
rs3764261 0.732 0.280 16 56959412 upstream gene variant C/A snv 0.31 26
rs11206510 0.763 0.240 1 55030366 intergenic variant T/A;C;G snv 16
rs602633 0.851 0.080 1 109278889 downstream gene variant T/G snv 0.63 10
rs8087799 0.882 0.080 18 22605468 regulatory region variant G/A snv 0.43 3
rs1795061 1.000 0.040 1 214235937 intergenic variant T/C;G snv 1
rs9316871 1.000 0.040 13 22287782 intergenic variant A/G snv 0.22 1
rs1799752
ACE
0.677 0.480 17 63488529 intron variant -/TTTTTTTTTTTGAGACGGAGTCTCGCTCTGTCGCCCATACAGTCACTTTT delins 25
rs77294580
ACE
1.000 0.040 17 63480396 missense variant G/A;T snv 4.0E-06; 4.0E-06 1
rs12692386 0.827 0.160 2 9555777 5 prime UTR variant A/G snv 0.72 5
rs1524668 0.851 0.160 2 9557243 upstream gene variant A/C snv 0.64 4
rs5186 0.630 0.560 3 148742201 3 prime UTR variant A/C snv 0.23 0.21 38
rs12695895 0.925 0.040 3 148725481 intron variant C/T snv 0.31 3
rs919433 0.882 0.080 2 197301841 intron variant G/A snv 0.38 3
rs7412 0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 47
rs1800469 0.547 0.760 19 41354391 intron variant A/G snv 0.69 78
rs2043211 0.653 0.480 19 48234449 missense variant A/T snv 0.33 0.29 29
rs12191786 0.851 0.120 6 22004398 intron variant C/A;T snv 4
rs3877899 0.827 0.160 5 42801166 missense variant C/A;T snv 4.0E-06; 0.20 7
rs7579 0.807 0.200 5 42800706 3 prime UTR variant C/T snv 0.31 0.26 6
rs1799864 0.572 0.680 3 46357717 missense variant G/A snv 0.13 0.12 68
rs1333049 0.614 0.520 9 22125504 intron variant G/C snv 0.41 60
rs10757278 0.620 0.520 9 22124478 intron variant A/G snv 0.40 44
rs10757274 0.701 0.320 9 22096056 intron variant A/G snv 0.41 22
rs2383207 0.695 0.280 9 22115960 intron variant A/G snv 0.64 22