Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs57045855 0.882 0.040 1 156134464 missense variant A/G;T snv 6
rs1553265736 0.925 0.040 1 156136080 missense variant G/C snv 4
rs61661343 0.851 0.040 1 156130687 missense variant T/C snv 4
rs138592977 1.000 0.040 1 156135968 missense variant G/A snv 5.6E-05 6.3E-05 3
rs201583907 0.925 0.040 1 156137191 missense variant G/A;C snv 8.6E-05 2
rs267607560 0.925 0.040 1 156115192 missense variant C/T snv 7.0E-06 2
rs28933092 1.000 0.040 1 156134497 missense variant A/G;T snv 2
rs1165819867 1.000 0.040 1 156134892 missense variant G/A;T snv 1
rs141490569 1.000 0.040 1 156136258 missense variant G/A snv 8.0E-05 9.8E-05 1
rs1553265180 1.000 0.040 1 156134500 missense variant T/A;G snv 1
rs1553265739 1.000 0.040 1 156136081 missense variant A/T snv 1
rs267607568 1.000 0.040 1 156115220 missense variant G/A;C;T snv 4.1E-06 1
rs267607572 1.000 0.040 1 156134518 missense variant T/G snv 1
rs267607574 1.000 0.040 1 156135916 missense variant G/A snv 1.6E-05 1.4E-05 1
rs58789393 1.000 0.040 1 156136010 missense variant G/A;T snv 4.0E-06 1
rs59065411 1.000 0.040 1 156115207 missense variant A/G snv 1
rs760318158 1.000 0.040 1 156126897 missense variant C/T snv 2.3E-04 6.3E-05 1
rs775964460 1.000 0.040 1 156134883 missense variant C/T snv 8.0E-06 1
rs267607581 0.925 0.080 1 156137651 splice region variant C/G snv 4
rs59301204 0.925 0.080 1 156135956 missense variant G/A;C snv 1.2E-05 4
rs397517907 0.925 0.080 1 156134914 missense variant C/T snv 4.0E-06 1.4E-05 2
rs4641 0.851 0.120 1 156137743 splice region variant C/T snv 0.26 0.21 6
rs56657623 0.827 0.120 1 156138540 missense variant G/A snv 1.6E-05 7.0E-06 5
rs56816490 0.925 0.120 1 156135913 stop gained G/A;T snv 4
rs267607578 0.925 0.120 1 156136952 missense variant G/A;C snv 1.4E-05 3