Variant (rsID / SNP)
rs34916635
rs34916635 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SDHB. Location: chromosome 1, position 17,371,298. Clinical significance in the table: Benign/Likely benign.
Reference-table entries
SDHBBenign
- Clinical significance (as recorded)
- Benign/Likely benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 1:17371298
- Cytoband
- 1p36.13
- HGVS
- NM_003000.3(SDHB):c.158G>A (p.Gly53Glu)
- Allele change
- Missense_G53E
Associated conditions / phenotypes
Hereditary cancer-predisposing syndrome|Carney-Stratakis syndrome|Hereditary pheochromocytoma-paraganglioma|Gastrointestinal stromal tumor|Cowden syndrome 1|Carney-Stratakis syndrome|Paragangliomas 4|Pheochromocytoma|Gastrointestinal stromal tumor|Paragangliomas 4|Pheochromocytoma
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.