Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs13107612 | 0.827 | 0.120 | 4 | 101818823 | intron variant | C/T | snv | 0.31 | 5 | ||
rs17199964 | 4 | 101786634 | intron variant | G/A;C | snv | 5 | |||||
rs13126505 | 1.000 | 0.040 | 4 | 101944147 | intron variant | G/A | snv | 4.1E-02 | 3 | ||
rs10028805 | 0.882 | 0.160 | 4 | 101816093 | intron variant | G/A | snv | 0.45 | 3 | ||
rs34592089 | 1.000 | 0.040 | 4 | 102005766 | intron variant | G/A;T | snv | 2 | |||
rs71597109 | 0.925 | 0.120 | 4 | 101819845 | intron variant | C/T | snv | 0.27 | 2 | ||
rs17248480 | 4 | 101514108 | intron variant | G/A | snv | 1.8E-02 | 2 | ||||
rs17031508 | 4 | 101639133 | intron variant | A/C | snv | 8.6E-02 | 1 | ||||
rs10516491 | 4 | 102031709 | intron variant | T/C | snv | 6.5E-02 | 1 | ||||
rs13127398 | 4 | 102000547 | intron variant | T/A | snv | 4.1E-02 | 1 | ||||
rs4637409 | 1.000 | 0.080 | 4 | 101832251 | intron variant | A/G | snv | 0.27 | 1 | ||
rs4426778 | 1.000 | 0.080 | 4 | 101859567 | intron variant | G/A;C | snv | 1 | |||
rs10516487 | 0.752 | 0.360 | 4 | 101829919 | missense variant | G/A;T | snv | 0.26; 8.0E-06 | 1 | ||
rs17266594 | 0.807 | 0.280 | 4 | 101829765 | intron variant | T/C | snv | 0.25 | 0.27 | 1 | |
rs34061204 | 4 | 101878992 | intron variant | A/-;AA;AAA | delins | 1 | |||||
rs6846071 | 4 | 101481058 | intron variant | T/G | snv | 0.15 | 1 | ||||
rs13109404 | 4 | 101975434 | intron variant | T/G | snv | 4.1E-02 | 1 |