Genetics University — Research, Education, Medical Genetics
Knowledge Hub

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.