Variant (rsID / SNP)

rs58639322

rs58639322 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ACADSB. Location: chromosome 10, position 124,800,121. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

ACADSBConflicting interpretations

Clinical significance (as recorded): Conflicting interpretations of pathogenicity
Variant type: single nucleotide variant
Chromosome / position: 10:124800121
Cytoband: 10q26.13
HGVS: NM_001609.4(ACADSB):c.443C>T (p.Thr148Ile)
Allele change: Missense_T148I

Associated conditions / phenotypes

Deficiency of 2-methylbutyryl-CoA dehydrogenase

Public references

dbSNP
ClinVar
Ensembl
gnomAD

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