Variant (rsID / SNP)

rs766667009

rs766667009 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SDHA. Location: chromosome 5, position 251,219. Clinical significance in the table: Pathogenic/Likely pathogenic.

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Reference-table entries

SDHAPathogenic

Clinical significance (as recorded): Pathogenic/Likely pathogenic
Variant type: single nucleotide variant
Chromosome / position: 5:251219
Cytoband: 5p15.33
HGVS: NM_004168.4(SDHA):c.1663+1G>T
Allele change: Silent

Associated conditions / phenotypes

Hereditary cancer-predisposing syndrome|Mitochondrial complex II deficiency, nuclear type 1|Paragangliomas 5

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.