Variant (rsID / SNP)

rs876659276

rs876659276 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SDHD. Location: chromosome 11, position 111,965,554. 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: 11:111965554
Cytoband: 11q23.1
HGVS: NM_003002.4(SDHD):c.340T>A (p.Tyr114Asn)
Allele change: Missense_Y75N

Associated conditions / phenotypes

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.