Source: GWASCAT
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs10127775 | 1 | 230160042 | intron variant | A/G;T | snv | 4 | |||||
rs10864728 | 1 | 230169168 | intron variant | A/G | snv | 0.50 | 3 | ||||
rs10489615 | 1 | 230169242 | intron variant | A/C;G | snv | 2 | |||||
rs1321257 | 1 | 230169566 | intron variant | G/A | snv | 0.50 | 2 | ||||
rs2144300 | 0.882 | 0.040 | 1 | 230159169 | intron variant | C/T | snv | 0.44 | 2 | ||
rs4846914 | 0.925 | 0.080 | 1 | 230159944 | intron variant | G/A | snv | 0.45 | 2 | ||
rs4846923 | 1 | 230171476 | intron variant | T/G | snv | 0.72 | 2 | ||||
rs17315646 | 1 | 230159560 | intron variant | C/A;G | snv | 0.45 | 1 | ||||
rs2281719 | 1.000 | 0.040 | 1 | 230161913 | intron variant | C/T | snv | 0.45 | 1 |