Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs6265 | 0.436 | 0.760 | 11 | 27658369 | missense variant | C/T | snv | 0.19 | 0.15 | 272 | |
rs759834365 | 0.448 | 0.760 | 11 | 27658456 | missense variant | C/T | snv | 1.2E-05 | 237 | ||
rs1056836 | 0.581 | 0.680 | 2 | 38071060 | missense variant | G/C | snv | 0.51 | 58 | ||
rs53576 | 0.641 | 0.320 | 3 | 8762685 | intron variant | A/G;T | snv | 42 | |||
rs1800440 | 0.653 | 0.440 | 2 | 38070996 | missense variant | T/C;G | snv | 0.15; 4.0E-06 | 29 | ||
rs41423247 | 0.695 | 0.440 | 5 | 143399010 | intron variant | G/C | snv | 0.31 | 23 | ||
rs2104425 | 0.925 | 0.040 | 6 | 40277470 | upstream gene variant | T/C | snv | 0.91 | 4 | ||
rs3842803 | 0.925 | 0.040 | 9 | 122392256 | synonymous variant | T/C | snv | 2.4E-02 | 8.2E-02 | 4 | |
rs466448 | 0.925 | 0.040 | 21 | 26171790 | intron variant | A/C;G | snv | 4 | |||
rs6432860 | 0.925 | 0.080 | 2 | 166041354 | synonymous variant | A/G;T | snv | 0.73; 4.0E-06 | 4 | ||
rs10809907 | 1.000 | 9 | 13134433 | non coding transcript exon variant | C/G;T | snv | 3 | ||||
rs1514280 | 1.000 | X | 15568325 | intron variant | A/G | snv | 3 |