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Variant (rsID / SNP)

rs772677312

PCSK9

rs772677312 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PCSK9. Location: chromosome 1, position 55,524,216. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

PCSK9Conflicting interpretations
Clinical significance (as recorded)
Conflicting interpretations of pathogenicity
Variant type
single nucleotide variant
Chromosome / position
1:55524216
Cytoband
1p32.3
HGVS
NM_174936.4(PCSK9):c.1399C>G (p.Pro467Ala)
Allele change
Missense_P467A

Associated conditions / phenotypes

Hypercholesterolemia, familial, 1|Hypercholesterolemia, autosomal dominant, 3|Hypobetalipoproteinemia|Familial hypercholesterolemia

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.