Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134
rs231775 0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 115
rs1267969615
ACE
0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 100
rs1222213359 0.574 0.720 6 43770966 missense variant G/A snv 62
rs1800471 0.597 0.840 19 41352971 missense variant C/G;T snv 5.6E-02 48
rs866294686 0.683 0.480 10 102657073 stop gained C/A;T snv 43
rs5742909 0.614 0.680 2 203867624 upstream gene variant C/T snv 6.7E-02 40
rs61747728 0.701 0.240 1 179557079 missense variant C/T snv 3.0E-02 2.8E-02 20
rs140511594 0.742 0.360 2 165941111 missense variant G/A snv 1.3E-04 1.1E-04 13
rs119473033 0.827 0.320 2 216478216 stop gained G/T snv 8.0E-05 1.3E-04 11
rs74315342 0.763 0.120 1 179561327 missense variant C/T snv 6.0E-04 5.3E-04 10
rs188942711 0.763 0.200 2 227253336 missense variant G/A;T snv 2.8E-05; 4.0E-06 9
rs748106387 0.851 0.240 2 216415427 stop gained C/A;T snv 2.8E-05 9
rs267602852
WT1
0.827 0.160 11 32417631 missense variant G/A snv 7
rs267607555 0.807 0.280 1 156136009 missense variant C/T snv 7.0E-06 6
rs530318579 0.807 0.080 1 179559710 missense variant C/T snv 1.4E-05 6
rs2239785 0.827 0.240 22 36265284 missense variant G/A snv 0.79 0.68 5
rs71785313 0.882 0.120 22 36265996 inframe deletion TTATAA/- delins 5
rs530391015 0.882 0.080 14 104703445 stop gained G/A;C;T snv 4.0E-06 5
rs753350907 0.827 0.080 10 100806499 missense variant G/A;C;T snv 4.0E-06; 4.0E-06 5
rs761613959 0.851 0.080 1 155187356 stop gained G/A snv 3.2E-05 7.0E-06 4
rs74315344 0.851 0.080 1 179575806 missense variant G/A snv 2.8E-03 4.2E-03 4
rs75462234 0.851 0.160 10 100749772 frameshift variant G/-;GG;GGG delins 4
rs114896482 0.882 0.080 19 35842487 missense variant G/A snv 2.3E-03 1.5E-03 3
rs779430565 0.882 0.080 11 101504316 missense variant T/A snv 1.2E-05 1.4E-05 3