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Variant (rsID / SNP)

rs73087649

COQ8A

rs73087649 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to COQ8A. Location: chromosome 1, position 227,172,236. 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
1:227172236
Cytoband
1q42.13
HGVS
NM_020247.5(COQ8A):c.1399-13G>A
Allele change
Silent

Associated conditions / phenotypes

Autosomal recessive cerebellar ataxia|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.