Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs769397961
ACE
0.882 0.120 17 63488758 missense variant G/A snv 1.2E-05 3.5E-05 4
rs1863918 0.882 0.160 5 179112381 3 prime UTR variant G/T snv 0.25 4
rs1229984 0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 83
rs1501299 0.597 0.720 3 186853334 intron variant G/C;T snv 52
rs2228079 0.882 0.160 1 203129147 synonymous variant T/G snv 0.31 0.26 4
rs2298383 0.827 0.200 22 24429543 non coding transcript exon variant C/A;T snv 11
rs1800035 0.925 0.080 10 111078794 missense variant C/G;T snv 1.9E-03 4
rs4994 0.578 0.640 8 37966280 missense variant A/G snv 0.11 9.2E-02 65
rs636832 0.790 0.400 1 35897874 intron variant G/A snv 0.23 8
rs5186 0.630 0.560 3 148742201 3 prime UTR variant A/C snv 0.23 0.21 38
rs2514259
AIP
0.807 0.280 11 67479201 upstream gene variant C/G;T snv 8
rs1937863 0.925 0.080 10 5009340 intron variant G/A;C;T snv 3
rs1800497 0.620 0.400 11 113400106 missense variant G/A snv 0.26 0.26 56
rs900418273 0.807 0.120 11 113393764 missense variant A/G snv 8
rs11824092 0.925 0.080 11 13324747 intron variant T/C snv 0.62 7
rs10766075 0.925 0.080 11 13297040 intron variant C/T snv 0.27 6
rs11022778 0.925 0.080 11 13369313 intron variant T/A;G snv 6
rs3789327 0.925 0.080 11 13363769 intron variant A/G snv 0.53 6
rs749437638 0.752 0.240 22 19968597 missense variant C/T snv 2.4E-05 1.4E-05 14
rs174697 0.851 0.080 22 19966309 intron variant A/G snv 0.88 5
rs1106634 0.851 0.080 8 20208538 intron variant G/A;C;T snv 0.18 5
rs33990840 0.925 0.080 1 206116320 missense variant C/G;T snv 5.0E-02; 2.8E-05 3
rs56164415 0.851 0.120 11 27700188 5 prime UTR variant G/A snv 5.9E-02 6
rs61888800 0.851 0.080 11 27700731 5 prime UTR variant G/T snv 0.19 5
rs759834365 0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237