Variant (rsID / SNP)

rs80292319

rs80292319 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ETFA. Location: chromosome 15, position 76,508,632. Clinical significance in the table: Benign.

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Reference-table entries

ETFABenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 15:76508632
Cytoband: 15q24.2
HGVS: NM_000126.4(ETFA):c.*268A>G
Allele change: Silent

Associated conditions / phenotypes

Multiple acyl-CoA dehydrogenase deficiency

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.