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Variant (rsID / SNP)

rs11039306

NDUFS3

rs11039306 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NDUFS3. Location: chromosome 11, position 47,605,859. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

NDUFS3Conflicting interpretations
Clinical significance (as recorded)
Conflicting interpretations of pathogenicity
Variant type
single nucleotide variant
Chromosome / position
11:47605859
Cytoband
11p11.2
HGVS
NM_004551.3(NDUFS3):c.628-7C>T
Allele change
Silent

Associated conditions / phenotypes

Leigh syndrome|Mitochondrial complex I deficiency, nuclear type 1

Public references

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