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Variant (rsID / SNP)

rs144867876

SDHAF2

rs144867876 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SDHAF2. Location: chromosome 11, position 61,205,157. 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
11:61205157
Cytoband
11q12.2
HGVS
NM_017841.4(SDHAF2):c.97C>T (p.Arg33Cys)
Allele change
Missense_R33C

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.