Genetics University — Research, Education, Medical Genetics
Knowledge Hub

Variant (rsID / SNP)

rs28362201

PCSK9

rs28362201 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PCSK9. Location: chromosome 1, position 55,505,266. Clinical significance in the table: Conflicting interpretations of pathogenicity.

ShareE-MailWhatsAppLinkedInXFacebookTelegram

Reference-table entries

PCSK9Conflicting interpretations
Clinical significance (as recorded)
Conflicting interpretations of pathogenicity
Variant type
single nucleotide variant
Chromosome / position
1:55505266
Cytoband
1p32.3
HGVS
NM_174936.4(PCSK9):c.-245G>T
Allele change
Silent

Associated conditions / phenotypes

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

Public references

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