Variant (rsID / SNP)

rs879254581

rs879254581 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LDLR. Location: chromosome 19, position 11,216,163. Clinical significance in the table: Pathogenic.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

LDLRPathogenic

Clinical significance (as recorded): Pathogenic
Variant type: Insertion
Chromosome / position: 19:11216163
Cytoband: 19p13.2
HGVS: NM_000527.5(LDLR):c.581_582insA (p.Ser194fs)

Associated conditions / phenotypes

Hypercholesterolemia, familial, 1

Public references

dbSNP
ClinVar
Ensembl
gnomAD

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