Variant (rsID / SNP)

rs6687605

rs6687605 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LDLRAP1. Location: chromosome 1, position 25,889,632. Clinical significance in the table: Benign.

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Reference-table entries

LDLRAP1Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 1:25889632
Cytoband: 1p36.11
HGVS: NM_015627.3(LDLRAP1):c.604T>C (p.Ser202Pro)
Allele change: Missense_S202P

Associated conditions / phenotypes

Hypercholesterolemia, familial, 4|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.