Variant (rsID / SNP)

rs267606611

rs267606611 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MT-CO3, MT-ATP6. Clinical significance in the table: Benign.

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Reference-table entries

MT-CO3Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Cytoband: -
HGVS: m.9438G>A

Associated conditions / phenotypes

Leber optic atrophy|Leigh 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.