Source: ALL
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs4925 | 0.677 | 0.560 | 10 | 104263031 | missense variant | C/A | snv | 0.25 | 0.23 | 28 | |
rs156697 | 0.672 | 0.560 | 10 | 104279427 | missense variant | A/G;T | snv | 0.35 | 25 | ||
rs866838052 | 0.851 | 0.160 | 7 | 143267618 | missense variant | C/A | snv | 6 | |||
rs62527607 | 0.827 | 0.160 | 8 | 103141321 | non coding transcript exon variant | G/T | snv | 0.14 | 5 | ||
rs11980379 | 0.882 | 0.120 | 7 | 50402283 | 3 prime UTR variant | T/C | snv | 0.25 | 3 | ||
rs189434316 | 0.925 | 0.120 | 14 | 92231568 | intergenic variant | A/T | snv | 4.1E-02 | 2 | ||
rs2393732 | 0.925 | 0.120 | 10 | 62007470 | intron variant | G/A | snv | 0.15 | 2 | ||
rs4948488 | 0.925 | 0.120 | 10 | 61925395 | intron variant | C/A;T | snv | 2 |