Variant (rsID / SNP)
rs182629842
rs182629842 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SDHC. Location: chromosome 1, position 161,332,301. Clinical significance in the table: Conflicting interpretations of pathogenicity.
Reference-table entries
SDHCConflicting interpretations
- Clinical significance (as recorded)
- Conflicting interpretations of pathogenicity
- Variant type
- single nucleotide variant
- Chromosome / position
- 1:161332301
- Cytoband
- 1q23.3
- HGVS
- NM_003001.5(SDHC):c.*78G>A
- Allele change
- Silent
Associated conditions / phenotypes
Hereditary pheochromocytoma-paraganglioma|Paragangliomas 3|Hereditary cancer-predisposing syndrome
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.