Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1051730 | 0.641 | 0.600 | 15 | 78601997 | synonymous variant | G/A | snv | 0.27 | 0.26 | 43 | |
rs16969968 | 0.653 | 0.360 | 15 | 78590583 | missense variant | G/A | snv | 0.26 | 0.24 | 37 | |
rs8034191 | 0.695 | 0.440 | 15 | 78513681 | intron variant | T/C | snv | 0.27 | 24 | ||
rs8040868 | 0.742 | 0.240 | 15 | 78618839 | synonymous variant | T/C | snv | 0.35 | 0.37 | 17 | |
rs6495308 | 0.851 | 0.160 | 15 | 78615314 | intron variant | T/C | snv | 0.29 | 8 | ||
rs1317286 | 0.925 | 0.120 | 15 | 78603787 | intron variant | A/G | snv | 0.30 | 6 | ||
rs3813567 | 1.000 | 0.080 | 15 | 78642209 | intron variant | G/A | snv | 0.77 | 2 |