Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs7229639 | 0.763 | 0.080 | 18 | 48924606 | intron variant | A/G | snv | 0.87 | 9 | ||
rs2178146 | 0.827 | 0.080 | 16 | 86430089 | downstream gene variant | T/C | snv | 0.31 | 5 | ||
rs2687201 | 0.925 | 0.080 | 3 | 70879779 | intergenic variant | A/C;G | snv | 5 | |||
rs4800353 | 0.925 | 0.080 | 18 | 22074176 | intergenic variant | A/G | snv | 0.30 | 5 | ||
rs3784262 | 0.882 | 0.160 | 15 | 57960908 | intron variant | T/A;C | snv | 5 | |||
rs11789015 | 0.882 | 0.080 | 9 | 93953746 | intron variant | A/C;G | snv | 5 | |||
rs10419226 | 0.925 | 0.080 | 19 | 18692362 | intron variant | T/G | snv | 0.67 | 5 | ||
rs7632500 | 0.925 | 0.080 | 3 | 168007561 | downstream gene variant | A/G | snv | 0.17 | 5 | ||
rs12035735 | 1 | 89839786 | intron variant | G/A | snv | 1.4E-03 | 4 | ||||
rs7240004 | 1.000 | 0.040 | 18 | 48868651 | intergenic variant | A/G | snv | 0.43 | 2 |