Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs11894252 | 0.925 | 0.120 | 2 | 46306237 | intron variant | T/A;C;G | snv | 3 | |||
rs1609682 | 0.882 | 0.160 | 2 | 112782628 | intron variant | G/T | snv | 0.70 | 3 | ||
rs2243267 | 0.882 | 0.160 | 5 | 132678194 | intron variant | G/A;C | snv | 3 | |||
rs2243289 | 0.882 | 0.240 | 5 | 132682440 | intron variant | A/G | snv | 0.26 | 0.23 | 3 | |
rs611646 | 0.882 | 0.120 | 11 | 108306370 | intron variant | T/A;C | snv | 3 | |||
rs10771279 | 0.925 | 0.120 | 12 | 26377610 | intron variant | T/A;C | snv | 0.40 | 2 | ||
rs1154454 | 0.925 | 0.120 | 4 | 99417185 | intron variant | A/G | snv | 0.22 | 2 | ||
rs11689011 | 1.000 | 0.120 | 2 | 46314037 | intron variant | T/A;C;G | snv | 2 | |||
rs1259293 | 0.925 | 0.120 | 3 | 120421014 | intron variant | T/C | snv | 0.59 | 2 | ||
rs12617313 | 0.925 | 0.120 | 2 | 46332637 | intron variant | A/G;T | snv | 2 | |||
rs2243270 | 0.925 | 0.120 | 5 | 132678417 | intron variant | A/G;T | snv | 2 | |||
rs2291599 | 0.925 | 0.120 | 11 | 11968352 | intron variant | T/C | snv | 0.83 | 0.85 | 2 | |
rs2499707 | 0.925 | 0.120 | 6 | 34085889 | intron variant | T/A;C | snv | 2 | |||
rs2504106 | 0.925 | 0.120 | 6 | 39854343 | intron variant | A/G | snv | 0.61 | 2 | ||
rs2761016 | 0.925 | 0.120 | 9 | 113391072 | intron variant | T/C | snv | 0.59 | 2 | ||
rs3889728 | 1.000 | 0.120 | 1 | 230713085 | intron variant | C/T | snv | 0.24 | 2 | ||
rs4381241 | 0.925 | 0.120 | 1 | 50441766 | intron variant | T/C | snv | 0.51 | 2 | ||
rs4765623 | 0.925 | 0.120 | 12 | 124836304 | intron variant | C/T | snv | 0.38 | 2 | ||
rs4787951 | 0.925 | 0.120 | 16 | 27332642 | intron variant | T/C | snv | 0.29 | 2 | ||
rs4903064 | 0.925 | 0.120 | 14 | 72812712 | intron variant | T/C | snv | 0.23 | 2 | ||
rs6641352 | 0.925 | 0.120 | X | 149711150 | intron variant | A/G | snv | 2 | |||
rs67311347 | 0.925 | 0.120 | 3 | 40491752 | intron variant | G/A | snv | 0.36 | 2 | ||
rs6937133 | 0.925 | 0.120 | 6 | 39832238 | intron variant | A/C;G | snv | 2 | |||
rs7102764 | 0.925 | 0.120 | 11 | 88778092 | intron variant | A/T | snv | 0.50 | 2 | ||
rs7396187 | 0.925 | 0.120 | 11 | 11967604 | intron variant | C/G | snv | 0.84 | 2 |