Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1057519783
ALK
0.851 0.080 2 29220747 missense variant C/T snv 10
rs1057519784
ALK
0.827 0.080 2 29220765 missense variant G/T snv 7
rs1057519861 0.776 0.080 7 55181398 missense variant T/A snv 15
rs10849605 0.882 0.080 12 955272 intron variant T/C snv 0.49 4
rs121913316 1.000 0.080 19 1220489 missense variant A/T snv 2
rs12587742 0.851 0.080 14 72926683 intron variant G/A snv 0.18 5
rs1275824108 0.851 0.080 14 54399922 missense variant A/G snv 7.0E-06 5
rs1329032366 0.882 0.080 4 94654530 missense variant A/G snv 4.0E-06 5
rs1389500636 0.827 0.080 7 55156796 missense variant G/A snv 6
rs139293 0.882 0.080 22 39100331 missense variant G/A;T snv 2.3E-04; 0.27 4
rs1423493595 0.851 0.080 20 50082836 missense variant G/A snv 4.0E-06 7.0E-06 5
rs1467453450 0.882 0.080 9 105506513 missense variant A/G snv 7.0E-06 4
rs1862214 0.882 0.080 19 32544943 intergenic variant G/A;C snv 4
rs200487215 0.882 0.080 16 75647605 missense variant T/A;C snv 1.6E-05 4
rs2036527 0.851 0.080 15 78559273 regulatory region variant G/A snv 0.29 12
rs2131877 0.827 0.080 3 195137645 intron variant G/A snv 0.20 6
rs374733251
MET
0.882 0.080 7 116740993 missense variant A/G snv 6.0E-05 7.7E-05 5
rs377444977 0.882 0.080 7 55143443 missense variant G/A snv 5.2E-05 2.1E-05 5
rs533748068 0.851 0.080 1 155950962 missense variant C/A;T snv 4.3E-06 7.0E-06 5
rs760943842 0.851 0.080 1 23362976 missense variant G/A snv 4.0E-05 1.4E-05 5
rs767935771
AXL
0.827 0.080 19 41259690 missense variant T/C snv 1.6E-05 5.6E-05 6
rs774352237 0.882 0.080 12 109908873 missense variant G/A snv 3.2E-05 2.1E-05 4
rs775057330 0.851 0.080 12 25149651 missense variant C/A;T snv 5
rs78768932
PXN
0.882 0.080 12 120222977 missense variant C/G;T snv 5.4E-03 5.4E-03 6
rs7969931 0.851 0.080 12 25089661 missense variant C/A;G snv 1.6E-05; 0.75 5