Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs71310379 3 179199003 missense variant C/A snv 4.4E-05 4.2E-05 1
rs756160717 3 12585204 missense variant G/A snv 1.2E-05 2.1E-05 1
rs7795743 7 55182437 non coding transcript exon variant G/A snv 0.56 1
rs779724499 12 54411885 missense variant G/A snv 1
rs867748453 7 140781608 missense variant G/A snv 1
rs946486 9 130770618 intron variant C/T snv 0.44 1
rs9879947 3 108046545 3 prime UTR variant G/A snv 0.45 1
rs1052667 0.882 0.040 19 47004177 3 prime UTR variant C/G;T snv 6
rs730882002 0.925 0.040 17 7674956 missense variant T/C snv 6
rs762471803 0.925 0.040 11 102114201 missense variant T/G snv 6
rs768949233 0.851 0.040 2 9490466 missense variant G/C;T snv 4.0E-06 5
rs8103851 0.851 0.040 19 53894400 intron variant C/G snv 0.44 5
rs11016879 0.882 0.040 10 129691518 intron variant A/C;G snv 0.66 4
rs1284410244 0.925 0.040 6 43778482 missense variant A/G snv 7.0E-06 4
rs7034162 0.882 0.040 9 14190288 intron variant A/T snv 0.81 4
rs7646409 0.882 0.040 3 179182405 intron variant T/C snv 0.26 4
rs765431049 0.925 0.040 7 93890271 missense variant C/T snv 1.6E-05 4
rs899706404 0.925 0.040 11 112087944 missense variant A/G snv 3
rs9397080 1.000 0.040 6 152059380 intron variant C/T snv 0.22 2
rs1131692237 1.000 0.040 17 39725161 missense variant T/G snv 1
rs1057519903 0.683 0.080 1 226064434 missense variant A/T snv 26
rs1057519904 0.742 0.080 6 27872233 missense variant T/A snv 14
rs1285136498 0.807 0.080 5 143400101 missense variant G/A snv 13
rs1553260624 0.763 0.080 1 226064454 missense variant G/A snv 13
rs1057519783
ALK
0.851 0.080 2 29220747 missense variant C/T snv 9