Source: GWASCAT
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1260326 | 0.645 | 0.600 | 2 | 27508073 | missense variant | T/C;G | snv | 0.63; 4.0E-06 | 0.68 | 55 | |
rs780094 | 0.658 | 0.400 | 2 | 27518370 | intron variant | T/C | snv | 0.67 | 35 | ||
rs780092 | 0.827 | 0.160 | 2 | 27520287 | intron variant | A/G | snv | 0.18 | 4 | ||
rs3817588 | 0.882 | 0.160 | 2 | 27508345 | intron variant | T/C | snv | 0.14 | 3 | ||
rs6547692 | 1.000 | 0.080 | 2 | 27512105 | intron variant | G/A | snv | 0.58 | 2 |