Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs7775478 | 1.000 | 0.040 | 6 | 65151300 | intron variant | G/T | snv | 0.26 | 1 | ||
rs2920283 | 0.925 | 0.040 | 8 | 142675619 | intron variant | T/C | snv | 0.44 | 2 | ||
rs16896391 | 1.000 | 0.040 | 6 | 65196105 | intron variant | T/C | snv | 0.23 | 1 | ||
rs28473387 | 1.000 | 0.040 | 8 | 142626112 | intergenic variant | T/C | snv | 0.63 | 1 | ||
rs7046863 | 1.000 | 0.040 | 9 | 133246054 | downstream gene variant | T/C | snv | 0.27 | 1 | ||
rs9297976 | 0.790 | 0.160 | 8 | 142670817 | intron variant | T/C;G | snv | 7 | |||
rs1036385 | 1.000 | 0.040 | 8 | 142761483 | upstream gene variant | T/C;G | snv | 1 | |||
rs2244163 | 1.000 | 0.040 | 8 | 142703082 | 3 prime UTR variant | T/G | snv | 0.42 | 0.43 | 1 |