Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1217691063 | 0.330 | 0.920 | 1 | 11796309 | missense variant | A/G | snv | 4.0E-06 | 7.0E-06 | 614 | |
rs28936670 | 0.708 | 0.280 | 5 | 173235011 | missense variant | G/A | snv | 3.4E-03 | 1.1E-02 | 17 | |
rs387906592 | 0.752 | 0.280 | 10 | 88941309 | missense variant | C/T | snv | 14 | |||
rs2277923 | 0.752 | 0.160 | 5 | 173235021 | synonymous variant | T/C | snv | 0.41 | 0.44 | 13 | |
rs766734961 | 0.851 | 0.160 | 10 | 88939548 | missense variant | C/A;T | snv | 4.0E-06 | 4 | ||
rs56166237 | 0.882 | 0.120 | 8 | 11708411 | missense variant | G/T | snv | 3.6E-03 | 2.0E-03 | 4 | |
rs6489957 | 0.925 | 0.120 | 12 | 114355808 | synonymous variant | G/A | snv | 4.4E-03 | 1.7E-02 | 4 | |
rs1383983021 | 0.882 | 0.160 | 2 | 88588014 | missense variant | T/C | snv | 3 | |||
rs368418329 | 0.925 | 0.120 | 8 | 11708019 | 5 prime UTR variant | G/T | snv | 5.9E-03 | 3 | ||
rs753571145 | 0.925 | 0.120 | 6 | 50823507 | missense variant | C/G | snv | 1.2E-05 | 2 |