Variant (rsID / SNP)

rs147859146

rs147859146 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MTR. Location: chromosome 1, position 237,062,395. Clinical significance in the table: Likely benign.

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Reference-table entries

MTRLikely benign

Clinical significance (as recorded): Likely benign
Variant type: single nucleotide variant
Chromosome / position: 1:237062395
Cytoband: 1q43
HGVS: NM_000254.3(MTR):c.*1451T>G
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.