"New York Genome Center"[submitter] AND "BDP1"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1696684	NM_018429.3(BDP1):c.6809-2A>G	BDP1	Single nucleotide variant (splice acceptor variant)	Hearing loss, autosomal recessive 112	GUncertain significance
Select item 1696685	NM_018429.3(BDP1):c.*1107T>C	BDP1	Single nucleotide variant (3 prime UTR variant)	Hearing loss, autosomal recessive 112	GUncertain significance