Variant (rsID / SNP)

rs1899

rs1899 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NDUFAF1. Location: chromosome 15, position 41,689,232. Clinical significance in the table: Benign.

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Reference-table entries

NDUFAF1Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 15:41689232
Cytoband: 15q15.1
HGVS: NM_016013.4(NDUFAF1):c.26G>A (p.Arg9His)
Allele change: Silent

Associated conditions / phenotypes

Mitochondrial complex I deficiency, nuclear type 1|Mitochondrial complex 1 deficiency, nuclear type 11

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.