Variant (rsID / SNP)

rs11265565

rs11265565 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NDUFS2. Location: chromosome 1, position 161,180,512. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

NDUFS2Benign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 1:161180512
Cytoband: 1q23.3
HGVS: NM_001377299.1(NDUFS2):c.986+12A>G
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.