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Variant (rsID / SNP)

rs199648872

NDUFA10

rs199648872 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NDUFA10. Location: chromosome 2, position 240,900,606. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

NDUFA10Conflicting interpretations
Clinical significance (as recorded)
Conflicting interpretations of pathogenicity
Variant type
single nucleotide variant
Chromosome / position
2:240900606
Cytoband
2q37.3
HGVS
NM_004544.4(NDUFA10):c.1000-3C>G
Allele change
Silent

Associated conditions / phenotypes

Mitochondrial complex I deficiency, nuclear type 1|Leigh syndrome

Public references

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