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Variant (rsID / SNP)

rs876658350

SDHAF2

rs876658350 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SDHAF2. Location: chromosome 11, position 61,205,562. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

SDHAF2Conflicting interpretations
Clinical significance (as recorded)
Conflicting interpretations of pathogenicity
Variant type
single nucleotide variant
Chromosome / position
11:61205562
Cytoband
11q12.2
HGVS
NM_017841.4(SDHAF2):c.347G>A (p.Trp116Ter)
Allele change
Nonsense_W116X

Associated conditions / phenotypes

Hereditary cancer-predisposing syndrome|Hereditary pheochromocytoma-paraganglioma

Public references

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