Variant (rsID / SNP)
rs34417623
rs34417623 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PCSK5. Location: chromosome 9, position 78,638,797. Clinical significance in the table: Uncertain significance.
Reference-table entries
PCSK5Uncertain significance
- Clinical significance (as recorded)
- Uncertain significance
- Variant type
- single nucleotide variant
- Chromosome / position
- 9:78638797
- Cytoband
- 9q21.13
- HGVS
- NM_001372043.1(PCSK5):c.555C>T (p.Tyr185=)
- Allele change
- Synonymous_Y185Y
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.