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Variant (rsID / SNP)

rs113652589

SDHAF2

rs113652589 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SDHAF2. Location: chromosome 11, position 61,213,555. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

SDHAF2Benign
Clinical significance (as recorded)
Benign/Likely benign
Variant type
single nucleotide variant
Chromosome / position
11:61213555
Cytoband
11q12.2
HGVS
NM_017841.4(SDHAF2):c.*12C>T
Allele change
Silent

Associated conditions / phenotypes

Hereditary pheochromocytoma-paraganglioma

Public references

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