Variant (rsID / SNP)
rs2479409
rs2479409 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PCSK9. Location: chromosome 1, position 55,504,650. Clinical significance in the table: Benign.
Reference-table entries
PCSK9Benign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 1:55504650
- Cytoband
- 1p32.3
- HGVS
- NM_174936.3(PCSK9):c.-861G>A
Associated conditions / phenotypes
Hypercholesterolemia, familial, 1
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.