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 | |
rs340005 | 15 | 60585831 | intron variant | G/A | snv | 0.67 | 3 | ||||
rs7310409 | 0.925 | 0.160 | 12 | 120987058 | intron variant | A/C;G;T | snv | 3 | |||
rs2393791 | 0.925 | 0.160 | 12 | 120986153 | intron variant | C/T | snv | 0.62 | 2 | ||
rs7979473 | 12 | 120982457 | intron variant | A/C;G | snv | 2 |