Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs267607277 | 0.807 | 0.120 | 14 | 90404386 | missense variant | A/G | snv | 6 | |||
rs398124647 | 0.807 | 0.120 | 2 | 47161851 | missense variant | T/A;C | snv | 6 | |||
rs794728708 | 0.827 | 0.120 | 1 | 237377386 | missense variant | G/A;T | snv | 8 | |||
rs121918598 | 0.851 | 0.080 | 1 | 237648523 | missense variant | G/A;C | snv | 4 | |||
rs190140598 | 0.851 | 0.120 | 1 | 237445488 | missense variant | C/A;T | snv | 1.2E-05 | 4 | ||
rs121918600 | 0.882 | 0.080 | 1 | 237791441 | missense variant | C/T | snv | 5 | |||
rs121918603 | 0.882 | 0.080 | 1 | 237639068 | missense variant | C/T | snv | 3 | |||
rs121918604 | 0.882 | 0.080 | 1 | 237798037 | missense variant | G/A;T | snv | 1.7E-05 | 3 | ||
rs1273246817 | 0.882 | 0.080 | 1 | 237784169 | missense variant | A/C | snv | 3 | |||
rs398124650 | 0.882 | 0.120 | 2 | 47161744 | missense variant | C/G;T | snv | 3 | |||
rs749547712 | 0.882 | 0.080 | 1 | 115768444 | missense variant | C/T | snv | 1.2E-05 | 3 | ||
rs773204795 | 0.882 | 0.120 | 4 | 64309896 | missense variant | C/T | snv | 2.4E-05 | 2.1E-05 | 3 | |
rs121918602 | 0.925 | 0.120 | 1 | 237454396 | missense variant | T/C | snv | 3 | |||
rs121918606 | 0.925 | 0.080 | 1 | 237819181 | missense variant | C/G | snv | 3 | |||
rs1458500258 | 0.925 | 0.080 | 1 | 237388098 | missense variant | G/T | snv | 7.0E-06 | 3 | ||
rs397515458 | 0.925 | 0.080 | 6 | 123503899 | stop gained | G/A | snv | 3.1E-05 | 5.6E-05 | 3 | |
rs794728721 | 0.925 | 0.080 | 1 | 237445489 | missense variant | G/A | snv | 3 | |||
rs1085307100 | 0.925 | 0.080 | 6 | 123512344 | frameshift variant | -/T | delins | 2 | |||
rs121434549 | 0.925 | 0.080 | 1 | 115705212 | missense variant | C/G;T | snv | 8.0E-06 | 2 | ||
rs121434550 | 0.925 | 0.080 | 1 | 115738256 | missense variant | A/T | snv | 2 | |||
rs121918597 | 0.925 | 0.080 | 1 | 237634937 | missense variant | C/T | snv | 2 | |||
rs121918599 | 0.925 | 0.080 | 1 | 237784024 | missense variant | C/G | snv | 2 | |||
rs121918601 | 0.925 | 0.120 | 1 | 237640938 | missense variant | A/T | snv | 2 | |||
rs121918605 | 0.925 | 0.080 | 1 | 237784314 | missense variant | A/G | snv | 2 | |||
rs267607276 | 0.925 | 0.080 | 14 | 90401385 | missense variant | A/G;T | snv | 2 |