Variant (rsID / SNP)

rs587776644

rs587776644 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SDHD. Location: chromosome 11, position 111,957,685. Clinical significance in the table: Likely pathogenic.

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Reference-table entries

SDHDLikely pathogenic

Clinical significance (as recorded): Likely pathogenic
Variant type: single nucleotide variant
Chromosome / position: 11:111957685
Cytoband: 11q23.1
HGVS: NM_003002.4(SDHD):c.52+2T>G
Allele change: Silent

Associated conditions / phenotypes

Paragangliomas 1|Pheochromocytoma

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.