Gene entry
SHMT1
serine hydroxymethyltransferase 1
- Chromosome
- 17
- Cytoband
- 17p11.2
- Variants (rsID)
- 11
SHMT1 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 17 (region 17p11.2). Its official name is “serine hydroxymethyltransferase 1”. The reference table lists 11 variants (rsID) for this gene.
Clinically classified variants
1 reference-table entries with clinical significance.
- rs1979277Uncertain significancesingle nucleotide variantGastrointestinal stromal tumor
Other listed variants
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.
