Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs141173114 | 1.000 | 0.080 | 6 | 10186099 | intron variant | G/A;T | snv | 1 | |||
rs11759950 | 1.000 | 0.080 | 6 | 10226000 | downstream gene variant | C/T | snv | 0.15 | 1 | ||
rs427754 | 1.000 | 0.080 | 18 | 10361780 | intron variant | T/A;C | snv | 1 | |||
rs206447 | 1.000 | 0.080 | 18 | 10439989 | intergenic variant | A/G | snv | 0.33 | 1 | ||
rs12509636 | 1.000 | 0.080 | 4 | 105089276 | intron variant | C/T | snv | 0.39 | 1 | ||
rs142020459 | 1.000 | 0.080 | 1 | 10512026 | intron variant | C/G | snv | 1.8E-02 | 1 | ||
rs9398035 | 1.000 | 0.080 | 6 | 105593507 | downstream gene variant | A/C | snv | 0.42 | 1 | ||
rs4946689 | 1.000 | 0.080 | 6 | 105753733 | intron variant | G/A | snv | 0.88 | 1 | ||
rs12214131 | 0.807 | 0.080 | 6 | 105760046 | intron variant | G/A | snv | 0.29 | 7 | ||
rs17035390 | 1.000 | 0.080 | 1 | 10593565 | intron variant | T/C | snv | 3.6E-02 | 1 | ||
rs2242288 | 1.000 | 0.080 | 1 | 10624041 | intron variant | C/A | snv | 4.6E-02 | 1 | ||
rs147170006 | 1.000 | 0.080 | 4 | 106590269 | intron variant | T/- | delins | 0.14 | 1 | ||
rs73837363 | 1.000 | 0.080 | 4 | 106622437 | intron variant | G/A | snv | 1 | |||
rs10516537 | 1.000 | 0.080 | 4 | 106706914 | intron variant | A/C | snv | 0.84 | 1 | ||
rs73667301 | 1.000 | 0.080 | 9 | 106865770 | intron variant | A/G | snv | 7.6E-02 | 1 | ||
rs59304342 | 1.000 | 0.080 | 1 | 10693037 | intron variant | T/A | snv | 5.0E-02 | 1 | ||
rs4109346 | 1.000 | 0.080 | 4 | 106967631 | intron variant | T/A | snv | 0.15 | 1 | ||
rs76067940 | 1.000 | 0.080 | 4 | 107131838 | intron variant | C/T | snv | 2.5E-02 | 1 | ||
rs9846246 | 1.000 | 0.080 | 3 | 107705243 | intron variant | G/A;T | snv | 1 | |||
rs76729432 | 1.000 | 0.080 | 8 | 107793457 | intergenic variant | T/C | snv | 5.7E-02 | 1 | ||
rs145562694 | 1.000 | 0.080 | 8 | 107806268 | intergenic variant | C/A;T | snv | 1 | |||
rs147906392 | 1.000 | 0.080 | 8 | 107894243 | intron variant | C/G;T | snv | 1 | |||
rs2047198 | 1.000 | 0.080 | 8 | 107950399 | intron variant | C/G;T | snv | 1 | |||
rs34657911 | 1.000 | 0.080 | 8 | 108081515 | intron variant | G/A | snv | 0.17 | 1 | ||
rs117769774 | 1.000 | 0.080 | 8 | 108090690 | intergenic variant | G/A | snv | 2.5E-02 | 1 |