Variant (rsID / SNP)

rs386829198

rs386829198 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MT-ND5. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

MT-ND5Benign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Cytoband: -
HGVS: NC_012920.1(MT-ND5):m.14002A>G

Associated conditions / phenotypes

Leigh syndrome

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.