ClinVar for MedGen (Select 463625) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 813832	9q21.11 duplication	TJP2	Duplication	Autosomal dominant nonsyndromic hearing loss 51	GPathogenic
Select item 236063	NC_000009.11:g.71705804_71974823invdup	TJP2	Duplication	Autosomal dominant nonsyndromic hearing loss 51	GPathogenic
Select item 236035	NC_000009.12:g.69090066_69225446dup	LOC124292588, LOC130001864 +4 more	Duplication	Autosomal dominant nonsyndromic hearing loss 51	GPathogenic

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