Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs746147592 1.000 0.160 X 100665627 missense variant G/A;C snv 5.5E-06 2
rs121909497 0.925 0.080 11 102955390 missense variant A/G snv 3
rs28939086 0.925 0.160 7 107690220 missense variant A/C;G snv 2.0E-04; 4.0E-06 4
rs671 0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 116
rs104894378 0.882 0.120 12 114385521 missense variant C/G;T snv 6
rs104894381 0.925 0.120 12 114401830 missense variant C/T snv 5
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs121918502 0.790 0.160 10 121517351 missense variant G/C snv 9
rs77543610 0.667 0.560 10 121520160 missense variant G/C snv 28
rs104894232 0.925 0.160 11 125900000 missense variant A/G snv 1.1E-03 1.0E-03 4
rs1057519321 0.807 0.160 5 128349391 missense variant C/A;T snv 7
rs4954218 0.925 0.080 2 135045855 intron variant G/T snv 0.83 5
rs4988235 0.752 0.400 2 135851076 intron variant G/A;C snv 19
rs1387329667 9 136500595 missense variant G/A snv 2
rs756434709 9 136514670 missense variant C/T snv 2.0E-05 7.0E-06 2
rs137854438 1.000 0.080 8 143728570 stop gained A/T snv 2
rs587777570 1.000 2 148947018 missense variant G/A snv 4
rs1799983 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs121912678 0.851 0.080 2 157774114 missense variant C/G;T snv 8
rs104893951 0.851 0.080 6 1610780 missense variant T/A;C snv 8.0E-06 5
rs142322800 1 161548502 missense variant T/C snv 1.5E-04 5.6E-05 1
rs1206736425 1 161626229 missense variant T/C snv 2
rs1057517786 0.925 0.400 3 167704889 stop gained G/A snv 3
rs121913483 0.649 0.560 4 1801841 missense variant C/A;G;T snv 4.2E-06; 1.3E-05 31