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Variant (rsID / SNP)

rs148035648

CPT2

rs148035648 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CPT2. Location: chromosome 1, position 53,675,699. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

CPT2Conflicting interpretations
Clinical significance (as recorded)
Conflicting interpretations of pathogenicity
Variant type
single nucleotide variant
Chromosome / position
1:53675699
Cytoband
1p32.3
HGVS
NM_000098.3(CPT2):c.353A>G (p.Asp118Gly)
Allele change
Missense_D118G

Associated conditions / phenotypes

Carnitine palmitoyltransferase II deficiency

Public references

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