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Gene entry

SDHC

succinate dehydrogenase complex subunit C

Chromosome
1
Cytoband
1q23.3
Variants (rsID)
33

SDHC is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 1 (region 1q23.3). Its official name is “succinate dehydrogenase complex subunit C”. The reference table lists 33 variants (rsID) for this gene.

Clinically classified variants

14 reference-table entries with clinical significance.

  • rs4600063Benignsingle nucleotide variantHereditary pheochromocytoma-paraganglioma
  • rs182629842Conflicting interpretationssingle nucleotide variantHereditary pheochromocytoma-paraganglioma|Paragangliomas 3|Hereditary cancer-predisposing syndrome
  • rs373731336Conflicting interpretationssingle nucleotide variantParagangliomas 3|Gastrointestinal stromal tumor|Paragangliomas 3|Hereditary cancer-predisposing syndrome
  • rs587778661Conflicting interpretationssingle nucleotide variantHereditary cancer-predisposing syndrome|Paragangliomas 3|Gastrointestinal stromal tumor|Hereditary pheochromocytoma-paraganglioma
  • rs786205147Conflicting interpretationssingle nucleotide variantCarney triad|Hereditary cancer-predisposing syndrome|Gastrointestinal stromal tumor|Paragangliomas 3
  • rs1057517818Likely pathogenicsingle nucleotide variantHereditary cancer-predisposing syndrome|Gastrointestinal stromal tumor|Paragangliomas 3
  • rs201286421Pathogenicsingle nucleotide variantParagangliomas 3|Hereditary cancer-predisposing syndrome|Hereditary pheochromocytoma-paraganglioma|Paragangliomas 3|Gastrointestinal stromal tumor
  • rs587776652Pathogenicsingle nucleotide variantParagangliomas 3|Paragangliomas 3|Gastrointestinal stromal tumor
  • rs587776653Pathogenicsingle nucleotide variantParagangliomas 3|Hereditary cancer-predisposing syndrome|Gastrointestinal stromal tumor|Paragangliomas 3
  • rs755235380Pathogenicsingle nucleotide variantParagangliomas 3|Hereditary cancer-predisposing syndrome|Gastrointestinal stromal tumor|Paragangliomas 3
  • rs786203457Pathogenicsingle nucleotide variantHereditary cancer-predisposing syndrome|Paragangliomas 3|Gastrointestinal stromal tumor|Gastrointestinal stromal tumor
  • rs786205146PathogenicDeletionCarney triad|Hereditary cancer-predisposing syndrome
  • rs876658301PathogenicDuplicationHereditary cancer-predisposing syndrome
  • rs148566767Uncertain significancesingle nucleotide variantGastrointestinal stromal tumor|Paragangliomas 3|Hereditary 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.