Variant (rsID / SNP)

rs882803

rs882803 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MMACHC. Location: chromosome 1, position 45,976,147. Clinical significance in the table: Benign.

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Reference-table entries

MMACHCBenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 1:45976147
Cytoband: 1p34.1
HGVS: NM_015506.3(MMACHC):c.*1260G>A
Allele change: Silent

Associated conditions / phenotypes

Disorders of Intracellular Cobalamin Metabolism

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.