Variant (rsID / SNP)

rs74614612

rs74614612 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NDUFA10. Location: chromosome 2, position 240,900,128. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

NDUFA10Benign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 2:240900128
Cytoband: 2q37.3
HGVS: NM_004544.4(NDUFA10):c.*407C>T
Allele change: Silent

Associated conditions / phenotypes

Leigh syndrome|Mitochondrial complex I deficiency, nuclear type 1

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.