Variant (rsID / SNP)

rs761683856

rs761683856 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LDLR. Location: chromosome 19, position 11,238,715. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

LDLRConflicting interpretations

Clinical significance (as recorded): Conflicting interpretations of pathogenicity
Variant type: single nucleotide variant
Chromosome / position: 19:11238715
Cytoband: 19p13.2
HGVS: NM_000527.5(LDLR):c.2343G>T (p.Glu781Asp)
Allele change: Missense_E603D

Associated conditions / phenotypes

Hypercholesterolemia, familial, 1|Familial hypercholesterolemia

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.