Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs3750716 | 0.925 | 0.120 | 10 | 100057106 | synonymous variant | C/G;T | snv | 6.6E-03 | 2 | ||
rs7750458 | 0.925 | 0.120 | 6 | 33077921 | intron variant | G/A | snv | 9.5E-02 | 2 | ||
rs9500928 | 0.925 | 0.120 | 6 | 33081917 | intron variant | C/T | snv | 4.0E-02 | 2 | ||
rs9501251 | 0.882 | 0.200 | 6 | 33081886 | intron variant | A/G | snv | 4.0E-02 | 3 | ||
rs9986765 | 0.925 | 0.120 | 7 | 143138146 | intron variant | A/G | snv | 0.12 | 3 | ||
rs1518364 | 0.925 | 0.120 | 2 | 197945251 | intron variant | G/A | snv | 0.49 | 3 | ||
rs938929 | 0.925 | 0.120 | 2 | 197916136 | intron variant | A/G | snv | 0.50 | 3 | ||
rs17000730 | 0.882 | 0.120 | 19 | 10380572 | 5 prime UTR variant | T/C | snv | 5.0E-03 | 3 | ||
rs280501 | 0.882 | 0.120 | 19 | 10380646 | upstream gene variant | C/T | snv | 0.20 | 3 | ||
rs7572733 | 0.925 | 0.120 | 2 | 198065082 | intron variant | C/T | snv | 0.43 | 4 | ||
rs2492358 | 0.851 | 0.160 | 9 | 34737831 | intron variant | C/T | snv | 0.78 | 5 | ||
rs3129843 | 0.827 | 0.160 | 6 | 32427949 | intergenic variant | A/G | snv | 6.3E-02 | 5 | ||
rs6738825 | 0.851 | 0.200 | 2 | 198032171 | intron variant | A/G | snv | 0.49 | 5 | ||
rs7812879 | 0.807 | 0.320 | 8 | 11482672 | upstream gene variant | T/A;C | snv | 6 | |||
rs10814916 | 0.851 | 0.200 | 9 | 4293150 | intron variant | A/C | snv | 0.57 | 7 | ||
rs10758593 | 0.827 | 0.240 | 9 | 4292083 | intron variant | G/A | snv | 0.45 | 8 | ||
rs1800451 | 0.776 | 0.240 | 10 | 52771466 | missense variant | C/T | snv | 3.2E-02 | 7.9E-02 | 9 | |
rs951005 | 0.807 | 0.200 | 9 | 34743684 | intron variant | G/A | snv | 0.78 | 10 | ||
rs11171739 | 0.807 | 0.320 | 12 | 56076841 | 5 prime UTR variant | C/T | snv | 0.49 | 10 | ||
rs280519 | 0.752 | 0.320 | 19 | 10362257 | splice region variant | A/C;G | snv | 0.50 | 10 | ||
rs5030737 | 0.752 | 0.360 | 10 | 52771482 | missense variant | G/A | snv | 5.6E-02 | 5.0E-02 | 11 | |
rs3733197 | 0.742 | 0.320 | 4 | 101918130 | missense variant | G/A | snv | 0.31 | 0.30 | 13 | |
rs2292239 | 0.742 | 0.480 | 12 | 56088396 | intron variant | T/G | snv | 0.65 | 13 | ||
rs2304256 | 0.732 | 0.360 | 19 | 10364976 | missense variant | C/A | snv | 0.27 | 0.23 | 13 | |
rs13277113 | 0.695 | 0.520 | 8 | 11491677 | intron variant | G/A | snv | 0.25 | 18 |