C1568248[trait identifier] AND "The Cell Therapy Center, The Universit - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 638640	NM_174878.3(CLRN1):c.433+1G>A	CLRN1	Single nucleotide variant (splice donor variant)	not provided +2 more	GPathogenic
Select item 633701	NM_174878.3(CLRN1):c.323T>C (p.Leu108Pro)	CLRN1 (L108P +1 more)	Single nucleotide variant (missense variant +2 more)	Usher syndrome type 3	GPathogenic