Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs365990 | 1.000 | 0.080 | 14 | 23392602 | missense variant | A/G | snv | 0.34 | 0.45 | 4 | |
rs10130976 | 1.000 | 0.080 | 14 | 22935497 | intron variant | T/A | snv | 0.12 | 1 | ||
rs869025519 | 1.000 | 0.080 | 3 | 38606037 | stop gained | C/A;T | snv | 4.0E-06 | 1 | ||
rs199473556 | 0.851 | 0.120 | 3 | 38630342 | missense variant | G/A | snv | 4 | |||
rs199473062 | 0.827 | 0.120 | 3 | 38622401 | stop gained | C/A;G;T | snv | 4.1E-06 | 5 | ||
rs387906656 | 0.807 | 0.120 | 14 | 23396970 | missense variant | G/A | snv | 2.1E-05 | 6 | ||
rs1805124 | 0.742 | 0.280 | 3 | 38603929 | missense variant | T/C | snv | 0.22 | 0.25 | 16 |