ClinVar Miner

List of variants reported as risk factor for Parkinson disease, mitochondrial

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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_000669.5(ADH1C):c.232G>T (p.Gly78Ter)	rs283413	0.00935
m.15950G>A	rs118203890
m.15965A>G	rs199474700

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