Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs3184504 | 0.572 | 0.600 | 12 | 111446804 | missense variant | T/A;C;G | snv | 0.67 | 61 | ||
rs10962692 | 0.925 | 0.120 | 9 | 16915876 | upstream gene variant | G/A;C | snv | 3 | |||
rs62274041 | 0.925 | 0.120 | 3 | 156717851 | upstream gene variant | G/A;T | snv | 3 | |||
rs3842727 | 1.000 | 0.120 | 11 | 2163618 | upstream gene variant | G/T | snv | 0.58 | 3 | ||
rs428595 | 1.000 | 0.120 | 22 | 21662102 | non coding transcript exon variant | A/G | snv | 0.98 | 3 | ||
rs4691139 | 1.000 | 0.120 | 4 | 164987569 | non coding transcript exon variant | A/G;T | snv | 2 |