Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs11231825 | 0.827 | 0.240 | 11 | 64592802 | synonymous variant | T/C | snv | 0.57 | 0.51 | 5 | |
rs16890979 | 0.827 | 0.200 | 4 | 9920543 | missense variant | C/T | snv | 0.24 | 0.29 | 7 | |
rs2054576 | 0.882 | 0.160 | 4 | 88107623 | intron variant | A/G | snv | 7.8E-02 | 4 | ||
rs2231142 | 0.583 | 0.680 | 4 | 88131171 | missense variant | G/C;T | snv | 4.0E-06; 0.12 | 56 | ||
rs2941484 | 0.882 | 0.160 | 8 | 75566533 | 3 prime UTR variant | C/T | snv | 0.52 | 4 | ||
rs3825016 | 0.882 | 0.160 | 11 | 64591814 | synonymous variant | C/T | snv | 0.57 | 0.51 | 3 | |
rs475688 | 0.882 | 0.160 | 11 | 64596819 | intron variant | C/T | snv | 0.25 | 3 | ||
rs505802 | 0.882 | 0.160 | 11 | 64589600 | upstream gene variant | T/C | snv | 0.45 | 4 | ||
rs671 | 0.529 | 0.840 | 12 | 111803962 | missense variant | G/A | snv | 1.9E-02 | 5.8E-03 | 116 | |
rs6837293 | 0.925 | 0.160 | 4 | 81141777 | intron variant | C/A;T | snv | 2 | |||
rs6855911 | 0.851 | 0.200 | 4 | 9934286 | intron variant | A/G | snv | 0.33 | 7 | ||
rs7688672 | 0.925 | 0.160 | 4 | 81148295 | intron variant | G/A | snv | 0.39 | 2 | ||
rs7903456 | 0.882 | 0.160 | 10 | 87159562 | intron variant | C/T | snv | 0.69 | 3 | ||
rs893006 | 0.882 | 0.160 | 11 | 64598324 | intron variant | C/A | snv | 0.61 | 3 |