Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1187323 | 0.882 | 0.080 | 9 | 84668501 | upstream gene variant | C/A;G;T | snv | 5 | |||
rs11904814 | 0.851 | 0.080 | 2 | 207562074 | intron variant | T/G | snv | 0.30 | 5 | ||
rs12630592 | 0.851 | 0.080 | 3 | 120049399 | intron variant | G/A;T | snv | 5 | |||
rs12936511 | 0.925 | 0.080 | 17 | 45807036 | synonymous variant | C/T | snv | 3.1E-02 | 3.0E-02 | 5 | |
rs13440581 | 0.882 | 0.080 | X | 151181399 | missense variant | A/G | snv | 0.45 | 0.45 | 5 | |
rs1415259 | 0.925 | 0.080 | 1 | 162115519 | intron variant | C/T | snv | 0.54 | 5 | ||
rs174697 | 0.851 | 0.080 | 22 | 19966309 | intron variant | A/G | snv | 0.88 | 5 | ||
rs2070587 | 0.882 | 0.080 | 12 | 108883967 | intron variant | T/G | snv | 0.32 | 5 | ||
rs2072115 | 0.882 | 0.080 | 12 | 47751585 | intron variant | A/C;G | snv | 5 | |||
rs228697 | 0.882 | 0.080 | 1 | 7827519 | missense variant | C/G | snv | 8.7E-02 | 7.3E-02 | 5 | |
rs3096140 | 0.882 | 0.080 | 5 | 37832731 | intron variant | G/A | snv | 0.69 | 5 | ||
rs496250 | 0.851 | 0.080 | 3 | 180909515 | intron variant | G/A | snv | 0.24 | 5 | ||
rs61888800 | 0.851 | 0.080 | 11 | 27700731 | 5 prime UTR variant | G/T | snv | 0.19 | 5 | ||
rs6903874 | 0.851 | 0.080 | 6 | 132575771 | downstream gene variant | T/C | snv | 0.23 | 5 | ||
rs7296288 | 0.851 | 0.080 | 12 | 49086185 | upstream gene variant | A/C | snv | 0.50 | 5 | ||
rs794727961 | 0.851 | 0.080 | 12 | 2512979 | missense variant | G/A | snv | 5 | |||
rs9825823 | 0.851 | 0.080 | 3 | 61096480 | intron variant | T/C | snv | 0.47 | 5 | ||
rs10223646 | 0.882 | 0.080 | 6 | 116296236 | intron variant | C/T | snv | 0.41 | 4 | ||
rs10848635 | 0.882 | 0.080 | 12 | 2207029 | intron variant | T/A;C | snv | 0.34 | 4 | ||
rs10988134 | 0.925 | 0.080 | 9 | 128833128 | 3 prime UTR variant | C/T | snv | 0.34 | 4 | ||
rs10997875 | 0.882 | 0.080 | 10 | 67920067 | downstream gene variant | T/A;C | snv | 4 | |||
rs112025902 | 0.925 | 0.080 | 4 | 120232669 | intron variant | A/G;T | snv | 4 | |||
rs115482041 | 0.925 | 0.080 | 9 | 4860267 | missense variant | C/T | snv | 2.6E-03 | 2.3E-03 | 4 | |
rs11911834 | 0.882 | 0.080 | 21 | 46602608 | 5 prime UTR variant | G/A;T | snv | 4 | |||
rs1402757753 | 0.882 | 0.080 | 12 | 132621913 | missense variant | G/A | snv | 7.0E-06 | 4 |