Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs11976235 | 1.000 | 7 | 100722758 | missense variant | C/T | snv | 3.5E-03 | 3.7E-03 | 1 | ||
rs149431976 | 1.000 | 7 | 100722991 | missense variant | C/G | snv | 9.1E-04 | 6.1E-04 | 1 | ||
rs62483572 | 1.000 | 7 | 100722010 | missense variant | G/A | snv | 2.4E-03 | 2.7E-03 | 1 | ||
rs137953994 | 1.000 | 7 | 100722667 | missense variant | G/A;C | snv | 1.0E-03; 5.3E-05 | 1 | |||
rs1358275550 | 1.000 | 7 | 100723081 | missense variant | G/A | snv | 4.0E-06 | 7.0E-06 | 1 |