Variant (rsID / SNP)

rs28357980

rs28357980 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MT-ND2, MT-CO1. Clinical significance in the table: Benign.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

MT-ND2Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Cytoband: -
HGVS: m.4917A>G

Associated conditions / phenotypes

Leber optic atrophy|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.