Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs745386663 0.807 0.160 3 33051956 missense variant G/A snv 8.0E-06 2.1E-05 4
rs6780220 0.882 0.120 3 33045708 non coding transcript exon variant A/C snv 0.19 3
rs72555392 0.807 0.200 3 33072613 missense variant C/T snv 3.6E-05 3
rs72555391 0.882 0.160 3 33016743 missense variant C/T snv 1.2E-05 2.1E-05 3
rs192732174 0.827 0.160 3 33068245 missense variant G/A;T snv 4.0E-05; 3.6E-05 2
rs72555363 0.925 0.160 3 33014263 missense variant C/A snv 2
rs72555390 0.807 0.160 3 33072637 missense variant A/G;T snv 2
rs72555362 0.925 0.160 3 33051979 missense variant C/A snv 5.6E-05 7.0E-06 2
rs761887139 0.925 0.160 3 33051997 missense variant G/C snv 4.0E-06 2
rs34421970 0.925 0.120 3 33018489 missense variant G/A snv 1.1E-02 9.4E-03 2
rs28934886 0.882 0.160 3 33016818 missense variant C/T snv 1.2E-05 2
rs189115557 0.882 0.160 3 33058220 missense variant C/T snv 6.4E-05 4.9E-05 1
rs376663785 0.827 0.160 3 33051989 missense variant A/C snv 1.6E-05 7.0E-06 1
rs73826339 1.000 0.120 3 33014196 missense variant T/A;C snv 4.7E-02 1
rs781658798 0.925 0.120 3 33046194 missense variant C/T snv 2.1E-05 1
rs755581184 1.000 0.120 3 32997206 missense variant G/A;T snv 8.0E-06 1
rs72555368 0.827 0.160 3 33014292 missense variant T/C snv 1.2E-05 1
rs201807974 1.000 0.120 3 32997296 missense variant G/A snv 1.2E-04 1.1E-04 1
rs1553612220 1.000 0.120 3 33068968 missense variant T/C snv 1
rs775958270 1.000 0.120 3 33051980 missense variant A/G snv 5.6E-05 7.0E-06 1
rs1356418704 1.000 0.160 3 32997112 missense variant G/A snv 1
rs754790691 1.000 0.080 3 33068890 missense variant C/G;T snv 4.0E-06; 8.0E-06 1
rs72555370 0.925 0.120 3 33072587 missense variant G/A snv 2.8E-05 2.8E-05 1
rs35289681 1.000 0.120 3 33068891 missense variant G/A snv 1.8E-02 1.6E-02 1
rs772155434 3 33058188 missense variant C/T snv 4.0E-06 1