Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs4765905 | 0.827 | 0.040 | 12 | 2240418 | intron variant | G/A;C | snv | 6 | |||
rs736707 | 0.851 | 0.040 | 7 | 103489956 | intron variant | A/G | snv | 0.30 | 6 | ||
rs2292305 | 0.882 | 0.080 | 15 | 39588621 | missense variant | A/C;G | snv | 4.0E-06; 0.16 | 4 | ||
rs850807 | 0.882 | 0.040 | 15 | 23652982 | intergenic variant | T/A;C | snv | 3 | |||
rs748128078 | 0.925 | 0.040 | 12 | 13562968 | missense variant | G/A | snv | 1.6E-05 | 5.6E-05 | 2 | |
rs756790727 | 0.925 | 0.040 | 12 | 13562883 | missense variant | G/A | snv | 1.2E-05 | 2 | ||
rs879254129 | 0.925 | 0.040 | 12 | 13562977 | missense variant | A/G | snv | 4.0E-06 | 2 |