Source: GWASCAT
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1169299 | 1.000 | 0.080 | 12 | 120991391 | intron variant | T/C | snv | 0.43 | 4 | ||
rs1183910 | 1.000 | 0.080 | 12 | 120983004 | intron variant | G/A | snv | 0.28 | 3 | ||
rs7310409 | 0.925 | 0.160 | 12 | 120987058 | intron variant | A/C;G;T | snv | 3 | |||
rs1800574 | 0.882 | 0.080 | 12 | 120979061 | missense variant | C/T | snv | 2.9E-02 | 2.2E-02 | 2 | |
rs2393791 | 0.925 | 0.160 | 12 | 120986153 | intron variant | C/T | snv | 0.62 | 2 | ||
rs12427353 | 1.000 | 0.080 | 12 | 120989098 | intron variant | G/A;C;T | snv | 1 | |||
rs1169288 | 0.776 | 0.160 | 12 | 120978847 | missense variant | A/C;T | snv | 0.35 | 8 |