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Variant (rsID / SNP)

rs587778661

SDHC

rs587778661 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SDHC. Location: chromosome 1, position 161,298,256. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

SDHCConflicting interpretations
Clinical significance (as recorded)
Conflicting interpretations of pathogenicity
Variant type
single nucleotide variant
Chromosome / position
1:161298256
Cytoband
1q23.3
HGVS
NM_003001.5(SDHC):c.148C>T (p.Arg50Cys)
Allele change
Silent

Associated conditions / phenotypes

Hereditary cancer-predisposing syndrome|Paragangliomas 3|Gastrointestinal stromal tumor|Hereditary pheochromocytoma-paraganglioma

Public references

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