Source: CURATED
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1006737 | 0.695 | 0.120 | 12 | 2236129 | intron variant | G/A | snv | 0.36 | 7 | ||
rs10744560 | 0.882 | 0.040 | 12 | 2277933 | intron variant | C/G;T | snv | 3 | |||
rs10774037 | 0.882 | 0.040 | 12 | 2311360 | intron variant | G/A | snv | 0.77 | 3 | ||
rs4765905 | 0.827 | 0.040 | 12 | 2240418 | intron variant | G/A;C | snv | 2 | |||
rs4765914 | 0.925 | 0.040 | 12 | 2311211 | intron variant | T/C;G | snv | 2 | |||
rs10774035 | 0.925 | 0.040 | 12 | 2259508 | intron variant | C/A;T | snv | 1 | |||
rs10848642 | 1.000 | 0.040 | 12 | 2222406 | non coding transcript exon variant | A/G | snv | 0.37 | 1 | ||
rs4765913 | 1.000 | 0.040 | 12 | 2310730 | intron variant | A/T | snv | 0.82 | 1 | ||
rs7297582 | 0.925 | 0.040 | 12 | 2246640 | intron variant | C/T | snv | 0.29 | 1 |