Variant (rsID / SNP)
rs6056609
rs6056609 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PLCB4. Location: chromosome 20, position 9,401,940. Clinical significance in the table: Benign.
Reference-table entries
PLCB4Benign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 20:9401940
- Cytoband
- 20p12.2
- HGVS
- NM_001377142.1(PLCB4):c.2155-4A>G
- 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.