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Variant (rsID / SNP)

rs144414842

HADHA

rs144414842 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to HADHA. Location: chromosome 2, position 26,462,021. Clinical significance in the table: Benign.

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Reference-table entries

HADHABenign
Clinical significance (as recorded)
Benign
Variant type
single nucleotide variant
Chromosome / position
2:26462021
Cytoband
2p23.3
HGVS
NM_000182.5(HADHA):c.68-10T>G
Allele change
Silent

Associated conditions / phenotypes

Mitochondrial trifunctional protein deficiency|Long chain 3-hydroxyacyl-CoA dehydrogenase deficiency|Mitochondrial trifunctional protein deficiency|Long chain 3-hydroxyacyl-CoA dehydrogenase deficiency

Public references

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