Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs113488022 | 0.351 | 0.840 | 7 | 140753336 | missense variant | A/C;G;T | snv | 4.0E-06 | 490 | ||
rs121913377 | 0.354 | 0.840 | 7 | 140753335 | missense variant | CA/AT;TT | mnv | 480 | |||
rs777980327 | 0.716 | 0.280 | 5 | 112837567 | missense variant | A/T | snv | 4.0E-06 | 7.0E-06 | 21 | |
rs1060503115 | 0.763 | 0.400 | 7 | 5978664 | missense variant | T/A;G | snv | 13 | |||
rs63750575 | 0.851 | 0.160 | 3 | 37047550 | missense variant | T/C | snv | 5 | |||
rs63751202 | 0.851 | 0.160 | 3 | 37048578 | missense variant | T/C;G | snv | 5 | |||
rs587778937 | 0.882 | 0.160 | 3 | 37040291 | missense variant | T/C;G | snv | 4 | |||
rs869312801 | 0.882 | 0.160 | 7 | 5987062 | missense variant | G/A;C;T | snv | 4.0E-06; 4.0E-06 | 4 |