Source: ALL
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs376612295 | 1.000 | 0.080 | 1 | 237454494 | missense variant | C/G | snv | 1.0E-04 | 7.0E-05 | 1 | |
rs79457258 | 1.000 | 0.080 | 1 | 237550629 | missense variant | G/A;C | snv | 8.4E-05 | 1 | ||
rs769219555 | 0.925 | 0.120 | 1 | 237648612 | missense variant | C/T | snv | 4.2E-05 | 8.4E-05 | 2 | |
rs189345192 | 1.000 | 0.080 | 1 | 237792207 | missense variant | G/A;C;T | snv | 3.6E-05 | 1 | ||
rs759830423 | 1.000 | 0.080 | 1 | 237445447 | missense variant | C/T | snv | 2.0E-05 | 2.1E-05 | 1 | |
rs121918604 | 0.882 | 0.080 | 1 | 237798037 | missense variant | G/A;T | snv | 1.7E-05 | 3 | ||
rs753733164 | 1.000 | 0.080 | 1 | 237784887 | missense variant | A/G | snv | 1.6E-05 | 2.8E-05 | 1 | |
rs190140598 | 0.851 | 0.120 | 1 | 237445488 | missense variant | C/A;T | snv | 1.2E-05 | 4 | ||
rs764772142 | 0.925 | 0.080 | 1 | 237377349 | missense variant | C/A;T | snv | 8.0E-06 | 2 | ||
rs371121679 | 1.000 | 0.080 | 1 | 237445471 | missense variant | G/A;T | snv | 8.0E-06 | 1 | ||
rs730880191 | 1.000 | 0.080 | 1 | 237566623 | missense variant | G/A | snv | 8.0E-06; 4.0E-06 | 1 | ||
rs1239093704 | 1.000 | 0.080 | 1 | 237759849 | missense variant | G/T | snv | 4.0E-06 | 1 | ||
rs730880196 | 1.000 | 0.080 | 1 | 237784037 | missense variant | A/C;G | snv | 4.0E-06 | 1 | ||
rs772220753 | 1.000 | 0.080 | 1 | 237640956 | missense variant | A/G | snv | 4.0E-06 | 1 | ||
rs1060500142 | 1.000 | 0.080 | 1 | 237330939 | missense variant | C/T | snv | 4.0E-06 | 1 | ||
rs794728708 | 0.827 | 0.120 | 1 | 237377386 | missense variant | G/A;T | snv | 8 | |||
rs121918600 | 0.882 | 0.080 | 1 | 237791441 | missense variant | C/T | snv | 5 | |||
rs121918598 | 0.851 | 0.080 | 1 | 237648523 | missense variant | G/A;C | snv | 4 | |||
rs121918602 | 0.925 | 0.120 | 1 | 237454396 | missense variant | T/C | snv | 3 | |||
rs121918603 | 0.882 | 0.080 | 1 | 237639068 | missense variant | C/T | snv | 3 | |||
rs121918606 | 0.925 | 0.080 | 1 | 237819181 | missense variant | C/G | snv | 3 | |||
rs1273246817 | 0.882 | 0.080 | 1 | 237784169 | missense variant | A/C | snv | 3 | |||
rs1458500258 | 0.925 | 0.080 | 1 | 237388098 | missense variant | G/T | snv | 7.0E-06 | 3 | ||
rs794728721 | 0.925 | 0.080 | 1 | 237445489 | missense variant | G/A | snv | 3 | |||
rs121918597 | 0.925 | 0.080 | 1 | 237634937 | missense variant | C/T | snv | 2 |