Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs758946412 | 0.821 | 0.214 | X | 100407506 | frameshift variant | C/CG | in-del | 5.6E-06 | 12 | ||
rs869312825 | 0.878 | 0.071 | 1 | 1804548 | start lost | T/C | snp | 11 | |||
rs869312826 | 0.923 | 0.071 | 1 | 1787378 | missense variant | C/T | snp | 6 | |||
rs74315390 | 0.744 | 0.107 | 20 | 63439609 | missense variant | C/G,T | snp | 5 | |||
rs121918622 | 0.784 | 0.071 | 2 | 165992332 | missense variant | C/A,T | snp | 4.0E-06 | 3 | ||
rs121908918 | 0.878 | 0.071 | 2 | 166284506 | stop gained | T/A | snp | 2.4E-05 | 2 | ||
rs1065852 | 0.756 | 0.250 | 22 | 42130692 | missense variant | G/A | snp | 0.21 | 0.19 | 2 | |
rs118192250 | 0.878 | 0.107 | 8 | 132175457 | missense variant | C/A | snp | 1 |