Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs564398 | 0.716 | 0.360 | 9 | 22029548 | 3 prime UTR variant | T/C | snv | 0.31 | 0.28 | 7 | |
rs1412829 | 0.742 | 0.400 | 9 | 22043927 | intron variant | A/G | snv | 0.28 | 6 | ||
rs3217992 | 0.683 | 0.480 | 9 | 22003224 | 3 prime UTR variant | C/T | snv | 0.32 | 6 | ||
rs4977756 | 0.683 | 0.440 | 9 | 22068653 | intron variant | G/A | snv | 0.64 | 5 | ||
rs523096 | 0.827 | 0.080 | 9 | 22019130 | intron variant | A/G | snv | 0.30 | 5 | ||
rs7049105 | 0.807 | 0.120 | 9 | 22028802 | intron variant | A/G | snv | 0.58 | 5 | ||
rs7865618 | 0.776 | 0.240 | 9 | 22031006 | non coding transcript exon variant | G/A;T | snv | 5 | |||
rs10120688 | 0.807 | 0.080 | 9 | 22056500 | intron variant | G/A | snv | 0.50 | 4 | ||
rs1063192 | 0.695 | 0.520 | 9 | 22003368 | 3 prime UTR variant | G/A;T | snv | 4 | |||
rs10965219 | 0.882 | 0.080 | 9 | 22053688 | intron variant | A/G | snv | 0.58 | 4 |