Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs121913502 | 0.708 | 0.320 | 15 | 90088702 | missense variant | C/A;T | snv | 3.2E-05 | 19 | ||
rs267606870 | 0.763 | 0.280 | 15 | 90088703 | missense variant | G/A;C | snv | 11 | |||
rs121434362 | 0.882 | 0.120 | 2 | 241767718 | missense variant | A/G | snv | 3 | |||
rs267606759 | 0.882 | 0.120 | 2 | 241751371 | missense variant | G/A;T | snv | 8.0E-06; 1.2E-05 | 3 | ||
rs1025426883 | 0.925 | 0.120 | 14 | 50247167 | missense variant | A/G | snv | 2 | |||
rs121434368 | 0.925 | 0.120 | 19 | 12899471 | missense variant | C/T | snv | 2 | |||
rs1277384196 | 0.925 | 0.120 | 19 | 12899507 | missense variant | T/C | snv | 4.0E-06 | 2 | ||
rs121434361 | 1.000 | 2 | 241742524 | missense variant | T/G | snv | 1 | ||||
rs145731647 | 1.000 | 2 | 241741010 | intron variant | A/G;T | snv | 4.0E-06; 1.4E-02 | 1 | |||
rs1559361049 | 1.000 | 2 | 241743772 | frameshift variant | T/- | delins | 1 | ||||
rs1559364994 | 1.000 | 2 | 241744879 | splice donor variant | T/C | snv | 1 | ||||
rs749330477 | 1.000 | 2 | 241741064 | frameshift variant | -/TC | delins | 1 | ||||
rs121434360 | 1.000 | 2 | 241767734 | missense variant | T/C | snv | 7.0E-06 | 1 | |||
rs587783517 | 1.000 | 2 | 241743697 | missense variant | C/T | snv | 1.6E-05 | 1.4E-05 | 1 | ||
rs753528947 | 1.000 | 2 | 241744707 | splice acceptor variant | A/G | snv | 2.4E-05 | 1.0E-04 | 1 |