Gene entry
GALNT12
polypeptide N-acetylgalactosaminyltransferase 12
- Chromosome
- 9
- Cytoband
- 9q22.33
- Variants (rsID)
- 19
GALNT12 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 9 (region 9q22.33). Its official name is “polypeptide N-acetylgalactosaminyltransferase 12”. The reference table lists 19 variants (rsID) for this gene.
Clinically classified variants
7 reference-table entries with clinical significance.
- rs1137654Benignsingle nucleotide variantHereditary cancer-predisposing syndrome
- rs41306504Benignsingle nucleotide variantHereditary cancer-predisposing syndrome|Colorectal cancer, susceptibility to, 1
- rs59362219Benignsingle nucleotide variantHereditary cancer-predisposing syndrome|Breast neoplasm
- rs145236923Conflicting interpretationssingle nucleotide variantHereditary cancer-predisposing syndrome|Adenomatous polyposis coli, attenuated|Colorectal cancer, susceptibility to, 1
- rs34565987Conflicting interpretationssingle nucleotide variantHereditary cancer-predisposing syndrome
- rs146834885Uncertain significancesingle nucleotide variantHereditary cancer-predisposing syndrome
- rs201499778Uncertain significancesingle nucleotide variantHereditary cancer-predisposing syndrome
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.