Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1557043622 | 0.695 | 0.400 | X | 48909843 | missense variant | C/A | snv | 46 | |||
rs121908132 | 0.851 | 0.240 | 9 | 32974544 | missense variant | A/C | snv | 4 | |||
rs767419411 | 0.882 | 0.200 | 1 | 161168069 | missense variant | G/A;C | snv | 1.2E-05; 8.0E-06 | 3 | ||
rs2290732 | 0.925 | 0.160 | 5 | 161897892 | 3 prime UTR variant | A/G;T | snv | 2 | |||
rs121908131 | 0.851 | 0.240 | 9 | 32984784 | missense variant | G/A | snv | 2.8E-05 | 7.0E-06 | 4 | |
rs757075712 | 0.763 | 0.200 | 10 | 58390856 | missense variant | C/T | snv | 1.6E-05 | 1.4E-05 | 15 | |
rs200482683 | 0.827 | 0.120 | 1 | 179552608 | missense variant | C/T | snv | 1.1E-04 | 1.1E-04 | 6 | |
rs74315342 | 0.763 | 0.120 | 1 | 179561327 | missense variant | C/T | snv | 6.0E-04 | 5.3E-04 | 10 | |
rs211037 | 0.742 | 0.240 | 5 | 162101274 | synonymous variant | C/T | snv | 0.28 | 0.31 | 14 |