Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1057519699 | 3 | 179218315 | missense variant | G/A | snv | 2 | |||||
rs1057519740 | 18 | 51065532 | missense variant | C/A | snv | 1 | |||||
rs1057519741 | 18 | 51078417 | missense variant | G/T | snv | 1 | |||||
rs1057519754 | 19 | 40236313 | missense variant | T/C | snv | 1 | |||||
rs1057519760 | 7 | 55160314 | missense variant | A/G | snv | 1 | |||||
rs121913326 | 5 | 112839729 | stop gained | G/T | snv | 1 | |||||
rs121913328 | 5 | 112839693 | stop gained | C/T | snv | 1 | |||||
rs121913329 | 5 | 112839726 | stop gained | C/T | snv | 1 | |||||
rs121913462 | 5 | 112839510 | stop gained | G/A;T | snv | 1 | |||||
rs1414521156 | 5 | 102459731 | missense variant | T/A;C | snv | 4.0E-06; 4.0E-06 | 1 | ||||
rs587780424 | 3 | 12433975 | missense variant | A/C | snv | 1 | |||||
rs74535574 | 5 | 112839879 | stop gained | C/A;T | snv | 1 | |||||
rs770292690 | 12 | 109908872 | missense variant | C/T | snv | 5.6E-05 | 9.8E-05 | 1 | |||
rs869312784 | 5 | 112838674 | missense variant | A/G | snv | 1 | |||||
rs11727676 | 0.776 | 0.080 | 4 | 144737912 | synonymous variant | T/C | snv | 6.6E-02 | 6.4E-02 | 14 | |
rs2070699 | 0.752 | 0.080 | 6 | 12292539 | intron variant | G/C;T | snv | 0.45 | 14 | ||
rs4925386 | 0.776 | 0.080 | 20 | 62345988 | intron variant | T/C | snv | 0.56 | 14 | ||
rs12916300 | 0.742 | 0.080 | 15 | 28165345 | intron variant | C/T | snv | 0.50 | 13 | ||
rs58658771 | 0.776 | 0.080 | 15 | 32709533 | intergenic variant | T/A | snv | 0.20 | 13 | ||
rs7229639 | 0.763 | 0.080 | 18 | 48924606 | intron variant | A/G | snv | 0.87 | 13 | ||
rs10821907 | 0.776 | 0.080 | 10 | 50888694 | upstream gene variant | C/T | snv | 0.20 | 12 | ||
rs4360494 | 0.776 | 0.080 | 1 | 37990219 | upstream gene variant | G/C | snv | 0.45 | 12 | ||
rs6058093 | 0.776 | 0.080 | 20 | 34625392 | intron variant | A/C | snv | 0.55 | 12 | ||
rs6584283 | 0.776 | 0.080 | 10 | 99530544 | intron variant | T/C | snv | 0.56 | 12 | ||
rs6691170 | 0.776 | 0.080 | 1 | 221872104 | intergenic variant | G/T | snv | 0.34 | 12 |