Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121909016 1.000 0.120 7 117540163 missense variant C/G snv 1
rs121909019 0.925 0.160 7 117611638 missense variant G/A;T snv 3.2E-05 1
rs121909020 1.000 0.120 7 117611640 missense variant G/A;C snv 4.0E-06 1
rs121909028 1.000 0.120 7 117642577 missense variant T/C snv 1
rs121909031 1.000 0.120 7 117530951 missense variant A/G snv 1
rs121909033 1.000 0.120 7 117592110 missense variant A/T snv 1
rs121909035 1.000 0.120 7 117603719 missense variant C/T snv 4.0E-06 1
rs121909036 0.925 0.160 7 117611635 missense variant T/C;G snv 1
rs121909037 1.000 0.120 7 117611653 missense variant A/C;G snv 4.0E-06 1
rs121909040 1.000 0.120 7 117642466 missense variant G/A snv 7.0E-06 1
rs121909041 1.000 0.120 7 117642483 missense variant T/A;C snv 4.0E-06 1
rs121909042 1.000 0.120 7 117652875 missense variant A/C;T snv 4.0E-06 1
rs121909044 0.925 0.200 7 117587812 missense variant G/A;C snv 4.0E-06 1
rs121909047 0.925 0.160 7 117590355 missense variant C/A snv 1.2E-05 2.1E-05 1
rs139304906 0.925 0.160 7 117611671 missense variant T/C snv 4.0E-06 7.0E-06 1
rs139468767 0.925 0.160 7 117592020 missense variant T/C snv 2.2E-05 1.6E-04 1
rs141033578 0.925 0.160 7 117606695 missense variant C/G;T snv 4.0E-06; 1.2E-05 1
rs142394380 0.925 0.160 7 117611622 missense variant G/C snv 4.0E-06 7.0E-06 1
rs143456784 1.000 0.120 7 117504324 missense variant C/T snv 1.2E-04 7.7E-05 1
rs143486492 1.000 0.120 7 117540120 missense variant G/A snv 5.7E-04 5.7E-04 1
rs145449046 0.925 0.160 7 117592541 stop gained C/G;T snv 1.3E-04; 5.5E-06 1
rs145540754 1.000 0.120 7 117592246 missense variant T/G snv 7.2E-05; 8.0E-06 3.1E-04 1
rs149353983 1.000 0.120 7 117504291 missense variant G/A;T snv 5.6E-05; 3.2E-05 1
rs150157202 0.925 0.120 7 117592427 missense variant G/A;T snv 1.8E-03 1.7E-03 1
rs150212784 1.000 0.120 7 117611595 missense variant T/C;G snv 4.0E-06; 6.5E-04 1