Variant (rsID / SNP)

rs187869948

rs187869948 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MMACHC. Location: chromosome 1, position 45,973,941. Clinical significance in the table: Uncertain significance.

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Reference-table entries

MMACHCUncertain significance

Clinical significance (as recorded): Uncertain significance
Variant type: single nucleotide variant
Chromosome / position: 1:45973941
Cytoband: 1p34.1
HGVS: NM_015506.3(MMACHC):c.334C>T (p.Arg112Cys)
Allele change: Missense_R55C

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.