Variant (rsID / SNP)
rs74772813
rs74772813 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PLCB4. Location: chromosome 20, position 9,460,659. Clinical significance in the table: Benign.
Reference-table entries
PLCB4Benign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 20:9460659
- Cytoband
- 20p12.2
- HGVS
- NM_001377142.1(PLCB4):c.*1003A>C
- Allele change
- Silent
Associated conditions / phenotypes
Auriculocondylar syndrome 2
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.