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Variant (rsID / SNP)

rs774789966

COQ8A

rs774789966 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to COQ8A. Location: chromosome 1, position 227,174,303. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

COQ8AConflicting interpretations
Clinical significance (as recorded)
Conflicting interpretations of pathogenicity
Variant type
single nucleotide variant
Chromosome / position
1:227174303
Cytoband
1q42.13
HGVS
NM_020247.5(COQ8A):c.1809C>T (p.Pro603=)
Allele change
Synonymous_P603P

Associated conditions / phenotypes

Coenzyme Q10 deficiency, Spinocerebellar Ataxia Type|Autosomal recessive ataxia due to ubiquinone deficiency

Public references

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