Variant (rsID / SNP)

rs876660368

rs876660368 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SDHB. Location: chromosome 1, position 17,350,462. Clinical significance in the table: Pathogenic/Likely pathogenic.

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Reference-table entries

SDHBPathogenic

Clinical significance (as recorded): Pathogenic/Likely pathogenic
Variant type: Deletion
Chromosome / position: 1:17350462
Cytoband: 1p36.13
HGVS: NM_003000.3(SDHB):c.642_642+6del

Associated conditions / phenotypes

Hereditary cancer-predisposing syndrome|Pheochromocytoma|Gastrointestinal stromal tumor|Paragangliomas 4

Public references

dbSNP
ClinVar
Ensembl
gnomAD

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.