Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs3184504 | 0.572 | 0.600 | 12 | 111446804 | missense variant | T/A;C;G | snv | 0.67 | 92 | ||
rs1260326 | 0.645 | 0.600 | 2 | 27508073 | missense variant | T/C;G | snv | 0.63; 4.0E-06 | 0.68 | 81 | |
rs34557412 | 0.763 | 0.240 | 17 | 16948873 | missense variant | A/G | snv | 3.5E-03 | 3.9E-03 | 15 | |
rs3731211 | 9 | 21986848 | intron variant | T/A | snv | 0.74 | 7 | ||||
rs142550358 | 9 | 88777772 | intron variant | CT/- | delins | 3.9E-02 | 5 | ||||
rs1354034 | 3 | 56815721 | intron variant | T/C | snv | 0.49 | 4 | ||||
rs10466905 | 12 | 6393666 | upstream gene variant | G/A | snv | 0.21 | 3 | ||||
rs149290349 | 2 | 43224818 | missense variant | G/A;T | snv | 6.7E-02 | 3 | ||||
rs2284344 | 12 | 6336163 | intron variant | G/C | snv | 0.49 | 2 | ||||
rs34038797 | 12 | 630843 | intron variant | C/G | snv | 0.42 | 2 |