Variant (rsID / SNP)

rs2853499

rs2853499 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MT-ND5, MT-ND4. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

MT-ND5Conflicting interpretations

Clinical significance (as recorded): Conflicting interpretations of pathogenicity
Variant type: single nucleotide variant
Cytoband: -
HGVS: NC_012920.1:m.12372G>A

Associated conditions / phenotypes

Mitochondrial disease

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.