Variant (rsID / SNP)
rs4600063
rs4600063 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SDHC. Location: chromosome 1, position 161,333,191. Clinical significance in the table: Benign.
Reference-table entries
SDHCBenign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 1:161333191
- Cytoband
- 1q23.3
- HGVS
- NM_003001.4(SDHC):c.*968A>G
- Allele change
- Silent
Associated conditions / phenotypes
Hereditary pheochromocytoma-paraganglioma
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.