Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1057519861 0.776 0.080 7 55181398 missense variant T/A snv 15
rs174577 1.000 0.080 11 61837342 intron variant C/A snv 0.38 13
rs2036527 0.851 0.080 15 78559273 regulatory region variant G/A snv 0.29 12
rs1057519783
ALK
0.851 0.080 2 29220747 missense variant C/T snv 10
rs56113850 0.807 0.080 19 40847202 intron variant T/C snv 0.52 10
rs6495309 0.807 0.080 15 78622903 upstream gene variant C/A;T snv 10
rs10937405 0.807 0.080 3 189665394 intron variant C/T snv 0.38 9
rs1458974438 0.807 0.080 19 1206957 missense variant G/A snv 9
rs10519203 0.851 0.080 15 78521704 intron variant G/A snv 0.67 8
rs1062980 0.827 0.080 15 78500185 3 prime UTR variant T/C snv 0.39 8
rs12910984 0.827 0.080 15 78599285 intron variant G/A;C;T snv 8
rs146795390 0.827 0.080 7 55191776 missense variant G/A snv 8.0E-06 7.0E-06 8
rs2036534 0.827 0.080 15 78534606 3 prime UTR variant T/C snv 0.26 8
rs6183
GHR
0.827 0.080 5 42718990 missense variant C/A snv 2.3E-03 7.4E-04 8
rs1057519784
ALK
0.827 0.080 2 29220765 missense variant G/T snv 7
rs1489759 0.882 0.080 4 144553321 intron variant A/G snv 0.43 7
rs2568494 0.851 0.080 15 78448622 intron variant G/A snv 0.36 7
rs7689420 0.851 0.080 4 144647200 non coding transcript exon variant T/C snv 0.79 7
rs931794 0.851 0.080 15 78533838 3 prime UTR variant G/A;C snv 7
rs938682 0.851 0.080 15 78604205 intron variant G/A snv 0.72 7
rs1057519729 0.827 0.080 15 66435113 missense variant A/C snv 6
rs11637630 0.882 0.080 15 78607377 intron variant G/A snv 0.71 6
rs12894467 0.807 0.080 14 101041390 non coding transcript exon variant C/T snv 0.51 0.50 6
rs1389500636 0.827 0.080 7 55156796 missense variant G/A snv 6
rs171140 0.807 0.080 19 45361744 non coding transcript exon variant C/A snv 0.58 0.64 6