Source: GWASDB
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs10168266 | 0.776 | 0.400 | 2 | 191071078 | intron variant | C/T | snv | 0.19 | 3 | ||
rs10174238 | 0.724 | 0.200 | 2 | 191108308 | intron variant | G/A | snv | 0.70 | 1 | ||
rs10181656 | 0.763 | 0.360 | 2 | 191105153 | intron variant | G/C | snv | 0.79 | 1 | ||
rs10931481 | 0.827 | 0.240 | 2 | 191090126 | intron variant | G/A | snv | 0.66 | 2 | ||
rs11889341 | 0.732 | 0.480 | 2 | 191079016 | intron variant | C/T | snv | 0.21 | 1 | ||
rs1517352 | 0.851 | 0.160 | 2 | 191066738 | intron variant | A/C | snv | 0.45 | 3 | ||
rs16833239 | 1.000 | 0.080 | 2 | 191075534 | intron variant | G/A | snv | 8.0E-02 | 1 | ||
rs3821236 | 0.882 | 0.160 | 2 | 191038032 | intron variant | G/A | snv | 0.25 | 3 | ||
rs7574865 | 0.574 | 0.720 | 2 | 191099907 | intron variant | T/G | snv | 0.79 | 8 | ||
rs7594501 | 1.000 | 0.080 | 2 | 191073874 | intron variant | G/A | snv | 8.7E-02 | 1 | ||
rs7601754 | 0.882 | 0.160 | 2 | 191075725 | intron variant | G/A;T | snv | 2 |