Related gene-specific medical variations for Gene (Select 126326) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3065869	NM_133261.3(GIPC3):c.592+2T>C	GIPC3	Single nucleotide variant (splice donor variant)	Autosomal recessive nonsyndromic hearing loss 15	GLikely pathogenic
Select item 2689130	NM_133261.3(GIPC3):c.103C>G (p.Pro35Ala)	GIPC3 (P35A)	Single nucleotide variant (missense variant)	Autosomal recessive nonsyndromic hearing loss 15	GUncertain significance