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Variant (rsID / SNP)

rs368469075

ACADS

rs368469075 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ACADS. Location: chromosome 12, position 121,177,107. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

ACADSConflicting interpretations
Clinical significance (as recorded)
Conflicting interpretations of pathogenicity
Variant type
single nucleotide variant
Chromosome / position
12:121177107
Cytoband
12q24.31
HGVS
NM_000017.4(ACADS):c.1095G>T (p.Gln365His)
Allele change
Missense_Q365H

Associated conditions / phenotypes

Deficiency of butyryl-CoA dehydrogenase

Public references

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