Source: GWASDB
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs2869967 | 0.827 | 0.120 | 4 | 88948181 | intron variant | T/C | snv | 0.49 | 5 | ||
rs7671167 | 0.925 | 0.040 | 4 | 88962828 | intron variant | C/T | snv | 0.53 | 4 | ||
rs1903003 | 0.925 | 0.080 | 4 | 88965146 | intron variant | C/G;T | snv | 3 | |||
rs2904259 | 4 | 88964563 | intron variant | T/A;C | snv | 3 | |||||
rs2045517 | 4 | 88949813 | intron variant | C/T | snv | 0.49 | 3 | ||||
rs2869966 | 1.000 | 0.040 | 4 | 88947927 | intron variant | C/T | snv | 0.47 | 3 | ||
rs2609255 | 0.882 | 0.080 | 4 | 88890044 | intron variant | G/T | snv | 0.73 | 1 |