Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs855791 0.701 0.400 22 37066896 missense variant A/G;T snv 0.57; 4.0E-06 38
rs4820268 0.851 0.160 22 37073551 missense variant G/A;C snv 0.53; 4.0E-06 14
rs11558492 0.827 0.200 1 231272345 missense variant A/G;T snv 0.16 5
rs1799945 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
rs111241405 0.925 0.120 2 238164165 missense variant G/T snv 4.7E-02 1.6E-02 2
rs1800562 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs1800730 0.649 0.480 6 26090957 missense variant A/T snv 1.0E-02 1.0E-02 32
rs11554495 0.701 0.240 12 52904798 missense variant C/A snv 4.9E-03 5.4E-03 19
rs7745236 1.000 0.040 6 7727292 missense variant C/G snv 4.9E-06; 4.1E-03 1.0E-02 1
rs11568350 0.790 0.240 2 189565370 missense variant C/A snv 3.8E-03 1.6E-02 9
rs137853920 0.925 0.080 9 117712970 missense variant G/A snv 2.3E-03 2.3E-03 2
rs41303501 0.882 0.080 7 100629279 missense variant C/T snv 1.9E-03 2.1E-03 3
rs35201683
HFE
0.732 0.360 6 26094205 stop gained C/A;T snv 1.4E-03 12
rs201062903 0.882 0.120 X 55013527 missense variant G/A snv 1.3E-03 1.2E-03 3
rs11568346 1.000 0.040 2 189561913 missense variant T/C snv 1.2E-03 4.9E-03 1
rs143496559
HJV
0.925 0.080 1 146018454 missense variant C/T snv 2.9E-04 5.2E-04 2
rs4986950 0.925 0.080 6 26092718 missense variant C/T snv 1.3E-04 7.0E-06 2
rs779021719 0.827 0.120 19 35284962 stop gained C/G;T snv 9.1E-05 5
rs768843272 0.925 0.080 7 100629298 missense variant T/C snv 8.4E-05 7.7E-05 2
rs121918367 0.827 0.080 12 50999214 missense variant C/A;T snv 6.0E-05 5
rs368420430 0.851 0.080 2 189564177 missense variant T/A;G snv 5.2E-05; 8.0E-06 4
rs80338891 0.851 0.080 7 100620889 missense variant C/T snv 4.8E-05 5.6E-05 4
rs202011978
HJV
0.925 0.080 1 146019446 missense variant G/A snv 4.7E-05 2.8E-04 2
rs781516027 0.882 0.080 6 26092744 missense variant C/G;T snv 8.0E-06; 3.6E-05 3
rs200488037 1.000 0.040 19 35285010 stop gained C/G;T snv 8.0E-06; 2.0E-05 1