Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1421085 | 0.752 | 0.280 | 16 | 53767042 | intron variant | T/C | snv | 0.31 | 28 | ||
rs1558902 | 0.827 | 0.120 | 16 | 53769662 | intron variant | T/A | snv | 0.31 | 21 | ||
rs1800437 | 0.827 | 0.160 | 19 | 45678134 | missense variant | G/C | snv | 0.18 | 0.17 | 13 | |
rs6567160 | 1.000 | 0.080 | 18 | 60161902 | upstream gene variant | T/C | snv | 0.21 | 12 | ||
rs7133378 | 12 | 123924955 | intron variant | G/A | snv | 0.38 | 6 | ||||
rs62104180 | 2 | 466003 | intergenic variant | G/A | snv | 2.9E-02 | 4 | ||||
rs6545714 | 2 | 59080590 | intron variant | G/A;C | snv | 4 | |||||
rs6755502 | 2 | 635721 | intergenic variant | T/C | snv | 0.85 | 3 |