Variant (rsID / SNP)

rs12654264

rs12654264 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to HMGCR. Location: chromosome 5, position 74,648,603. Clinical significance in the table: association.

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Reference-table entries

HMGCRAssociation

Clinical significance (as recorded): association
Variant type: single nucleotide variant
Chromosome / position: 5:74648603
Cytoband: 5q13.3
HGVS: NM_000859.3(HMGCR):c.1368+1176A>T
Allele change: Silent

Associated conditions / phenotypes

Low density lipoprotein cholesterol level quantitative trait locus 3

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.