Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs11004733 | 0.882 | 0.040 | 10 | 55089584 | intron variant | C/T | snv | 2.9E-02 | 4 | ||
rs141252918 | 0.882 | 0.040 | 6 | 151506923 | intron variant | G/A;C | snv | 4 | |||
rs149268645 | 0.882 | 0.040 | 2 | 202968295 | intron variant | G/A | snv | 8.4E-02 | 4 | ||
rs4870888 | 0.882 | 0.040 | 8 | 124096736 | intron variant | T/C | snv | 0.39 | 4 | ||
rs62173322 | 0.882 | 0.040 | 2 | 169754519 | intron variant | A/G | snv | 0.32 | 4 | ||
rs76371172 | 0.882 | 0.040 | 15 | 31522252 | intron variant | T/G | snv | 9.1E-03 | 4 | ||
rs9577511 | 0.882 | 0.040 | 13 | 113337508 | intron variant | A/G | snv | 0.15 | 4 | ||
rs17173608 | 0.807 | 0.240 | 7 | 150339575 | intron variant | T/G | snv | 0.11 | 3 | ||
rs17387100 | 0.925 | 0.040 | 4 | 15993502 | intron variant | A/G | snv | 7.5E-02 | 3 | ||
rs26318 | 0.925 | 0.040 | 5 | 116352208 | intron variant | C/T | snv | 0.99 | 3 | ||
rs300774 | 0.925 | 0.040 | 2 | 112496 | intergenic variant | A/C;T | snv | 2 | |||
rs7296262 | 1.000 | 0.040 | 12 | 128610527 | intron variant | T/C;G | snv | 2 |