Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1259560536 | 1.000 | 0.040 | 20 | 3671756 | missense variant | T/C | snv | 7.0E-06 | 1 | ||
rs1402272180 | 1.000 | 0.040 | 1 | 243637661 | missense variant | C/T | snv | 7.0E-06 | 1 | ||
rs770462360 | 1.000 | 0.040 | 11 | 64839070 | missense variant | G/A | snv | 2.0E-05 | 1 | ||
rs1384093596 | 1.000 | 0.040 | 12 | 67657500 | missense variant | C/T | snv | 1 | |||
rs779221554 | 1.000 | 0.040 | X | 109430395 | missense variant | C/A;T | snv | 1 | |||
rs375412266 | 1.000 | 0.040 | 3 | 50617647 | missense variant | C/G;T | snv | 2.1E-04; 4.1E-06 | 1 | ||
rs17855787 | 1.000 | 0.040 | 17 | 50109341 | missense variant | G/A | snv | 1 | |||
rs371854396 | 1.000 | 0.040 | 1 | 20638098 | missense variant | C/G;T | snv | 1.6E-05; 4.0E-06 | 1 | ||
rs1466858740 | 1.000 | 0.040 | 16 | 24180881 | missense variant | G/A | snv | 1 | |||
rs1567176006 | 1.000 | 0.040 | 16 | 3602208 | frameshift variant | CT/- | del | 1 | |||
rs757496714 | 1.000 | 0.040 | 20 | 388189 | missense variant | C/T | snv | 4.0E-06 | 1 | ||
rs2291427 | 0.925 | 0.040 | 10 | 45440776 | intron variant | A/G;T | snv | 2 | |||
rs11548193 | 0.925 | 0.040 | 19 | 48799813 | missense variant | G/A;C | snv | 0.14 | 2 | ||
rs11670188 | 0.925 | 0.040 | 19 | 2014038 | non coding transcript exon variant | A/G | snv | 0.16 | 2 | ||
rs1210653597 | 0.925 | 0.120 | 9 | 21968756 | missense variant | T/C | snv | 2 | |||
rs1558650888 | 0.925 | 0.040 | 2 | 25234308 | missense variant | G/A | snv | 2 | |||
rs9642393 | 0.925 | 0.040 | 7 | 55177954 | intron variant | T/C | snv | 0.24 | 2 | ||
rs7325927 | 0.925 | 0.040 | 13 | 107823165 | intron variant | C/T | snv | 0.38 | 2 | ||
rs3829382 | 0.925 | 0.040 | 13 | 28003551 | 3 prime UTR variant | G/T | snv | 0.46 | 2 | ||
rs11558961 | 0.925 | 0.040 | 17 | 44907319 | 3 prime UTR variant | G/C;T | snv | 0.27; 1.2E-05 | 2 | ||
rs759927375 | 0.925 | 0.040 | 6 | 26020589 | missense variant | G/A;C | snv | 1.2E-05; 8.0E-06 | 2 | ||
rs1161136341 | 0.925 | 0.080 | 7 | 18591621 | missense variant | G/A | snv | 8.0E-06 | 1.4E-05 | 2 | |
rs774238794 | 0.925 | 0.080 | 7 | 18644690 | missense variant | G/A;T | snv | 4.1E-05; 4.1E-06 | 2 | ||
rs8957 | 0.925 | 0.040 | 20 | 63742354 | missense variant | G/T | snv | 0.71 | 0.78 | 2 | |
rs7732320 | 0.925 | 0.040 | 5 | 81423306 | intron variant | C/T | snv | 0.22 | 2 |