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Variant (rsID / SNP)

rs149201273

NDUFS8

rs149201273 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NDUFS8. Location: chromosome 11, position 67,803,806. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

NDUFS8Conflicting interpretations
Clinical significance (as recorded)
Conflicting interpretations of pathogenicity
Variant type
single nucleotide variant
Chromosome / position
11:67803806
Cytoband
11q13.2
HGVS
NM_002496.4(NDUFS8):c.459C>T (p.Cys153=)
Allele change
Synonymous_C153C

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.