Variant (rsID / SNP)
rs3738547
rs3738547 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MTR. Location: chromosome 1, position 236,958,937. Clinical significance in the table: Benign.
Reference-table entries
MTRBenign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 1:236958937
- Cytoband
- 1q43
- HGVS
- NM_000254.3(MTR):c.-67C>T
- Allele change
- Silent
Associated conditions / phenotypes
Disorders of Intracellular Cobalamin Metabolism
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.