Variant (rsID / SNP)

rs587776647

rs587776647 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SDHD. Location: chromosome 11, position 111,965,677. Clinical significance in the table: Uncertain significance.

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Reference-table entries

SDHDUncertain significance

Clinical significance (as recorded): Uncertain significance
Variant type: Deletion
Chromosome / position: 11:111965677
Cytoband: 11q23.1
HGVS: NM_003002.4(SDHD):c.463del (p.Met155fs)

Associated conditions / phenotypes

Paragangliomas 1|Hereditary cancer-predisposing syndrome

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.