Variant (rsID / SNP)

rs878854574

rs878854574 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SDHB. Location: chromosome 1, position 17,359,642. Clinical significance in the table: Likely pathogenic.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

SDHBLikely pathogenic

Clinical significance (as recorded): Likely pathogenic
Variant type: single nucleotide variant
Chromosome / position: 1:17359642
Cytoband: 1p36.13
HGVS: NM_003000.3(SDHB):c.201-2A>C
Allele change: Silent

Associated conditions / phenotypes

Paragangliomas 4|Gastrointestinal stromal tumor|Pheochromocytoma

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.