Variant (rsID / SNP)
rs876658301
rs876658301 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SDHC. Location: chromosome 1, position 161,326,600. Clinical significance in the table: Pathogenic.
Reference-table entries
SDHCPathogenic
- Clinical significance (as recorded)
- Pathogenic
- Variant type
- Duplication
- Chromosome / position
- 1:161326600
- Cytoband
- 1q23.3
- HGVS
- NM_003001.5(SDHC):c.376dup (p.Tyr126fs)
Associated conditions / phenotypes
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.