ClinVar Miner

List of variants reported as uncertain significance for Autosomal recessive optic atrophy, OPA7 type by Institute of Human Genetics, University of Goettingen

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Total variants: 1

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HGVS	dbSNP	gnomAD frequency
NM_032273.4(TMEM126A):c.329G>A (p.Gly110Asp)	rs374124838

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