Variant (rsID / SNP)

rs8108064

rs8108064 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NDUFA11. Location: chromosome 19, position 5,903,807. Clinical significance in the table: Benign.

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Reference-table entries

NDUFA11Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 19:5903807
Cytoband: 19p13.3
HGVS: NM_175614.4(NDUFA11):c.-88C>A
Allele change: Silent

Associated conditions / phenotypes

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.