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Variant (rsID / SNP)

rs137853960

LDLR

rs137853960 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LDLR. Location: chromosome 19, position 11,210,979. 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
19:11210979
Cytoband
19p13.2
HGVS
NM_000527.5(LDLR):c.148G>T (p.Ala50Ser)
Allele change
Missense_A50S

Associated conditions / phenotypes

Hypercholesterolemia, familial, 1|Familial hypercholesterolemia|Hypercholesterolemia

Public references

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