ClinVar Miner

List of variants in gene combination NDUFS8, TCIRG1 reported as uncertain significance for Leigh syndrome

Included ClinVar conditions (9):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 1
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HGVS dbSNP
NM_002496.4(NDUFS8):c.*40A>G rs61329983

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