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Variant (rsID / SNP)

rs121908419

ACAD8

rs121908419 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ACAD8. Location: chromosome 11, position 134,132,450. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

ACAD8Conflicting interpretations
Clinical significance (as recorded)
Conflicting interpretations of pathogenicity
Variant type
single nucleotide variant
Chromosome / position
11:134132450
Cytoband
11q25
HGVS
NM_014384.3(ACAD8):c.1129G>A (p.Gly377Ser)
Allele change
Missense_G377S

Associated conditions / phenotypes

Deficiency of isobutyryl-CoA dehydrogenase

Public references

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