Variant (rsID / SNP)
rs111430410
rs111430410 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SDHB. Location: chromosome 1, position 17,380,483. 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
- 1:17380483
- Cytoband
- 1p36.13
- HGVS
- NM_003000.3(SDHB):c.32G>A (p.Arg11His)
- Allele change
- Missense_R11H
Associated conditions / phenotypes
Renal cell carcinoma, papillary, 1|Gastrointestinal stromal tumor|Paragangliomas 4|Pheochromocytoma|Hereditary pheochromocytoma-paraganglioma|Hereditary cancer-predisposing syndrome|Paragangliomas 4|Gastrointestinal stromal tumor|Paraganglioma|Pheochromocytoma|Pheochromocytoma|Paraganglioma
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.