Source: CLINVAR
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1560739587 | 4 | 140396131 | missense variant | T/C | snv | 1 | |||||
rs1560743601 | 4 | 140405975 | missense variant | G/T | snv | 1 | |||||
rs201306926 | 4 | 140399004 | missense variant | T/C | snv | 3.6E-05 | 7.0E-06 | 1 |