Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs116843064 | 0.776 | 0.160 | 19 | 8364439 | missense variant | G/A | snv | 1.3E-02 | 1.5E-02 | 16 | |
rs198851 | 6 | 26104404 | downstream gene variant | T/A;C;G | snv | 15 | |||||
rs2954021 | 1.000 | 0.040 | 8 | 125469835 | intron variant | A/G | snv | 0.54 | 15 | ||
rs112259268 | 17 | 43797377 | downstream gene variant | C/A | snv | 1.9E-02 | 6 | ||||
rs62434129 | 6 | 150687701 | intron variant | A/G;T | snv | 8.8E-02 | 6 | ||||
rs1799852 | 3 | 133756878 | synonymous variant | C/T | snv | 0.13 | 0.11 | 5 | |||
rs7140110 | 13 | 113841051 | non coding transcript exon variant | T/C | snv | 0.28 | 4 |