Variant (rsID / SNP)

rs370382601

rs370382601 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ACSF3. Location: chromosome 16, position 89,167,090. Clinical significance in the table: Pathogenic/Likely pathogenic.

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Reference-table entries

ACSF3Pathogenic

Clinical significance (as recorded): Pathogenic/Likely pathogenic
Variant type: single nucleotide variant
Chromosome / position: 16:89167090
Cytoband: 16q24.3
HGVS: NM_001243279.3(ACSF3):c.1A>G (p.Met1Val)
Allele change: Missense_M1V

Associated conditions / phenotypes

Combined malonic and methylmalonic acidemia

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.