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Variant (rsID / SNP)

rs144018609

CYP27A1

rs144018609 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CYP27A1. Location: chromosome 2, position 219,677,420. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

CYP27A1Conflicting interpretations
Clinical significance (as recorded)
Conflicting interpretations of pathogenicity
Variant type
single nucleotide variant
Chromosome / position
2:219677420
Cytoband
2q35
HGVS
NM_000784.4(CYP27A1):c.792G>A (p.Val264=)
Allele change
Synonymous_V264V

Associated conditions / phenotypes

Cholestanol storage disease

Public references

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