Related gene-specific medical variations for Gene (Select 2615) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1676660	NM_001370189.1(LRRC32):c.9C>A (p.Cys3Ter)	LRRC32 (C3*)	Single nucleotide variant	Cleft palate, proliferative retinopathy, and developmental delay	GLikely pathogenic
Select item 226215	GRCh37/hg19 11q13.5(chr11:76268060-76417696)	LRRC32	Copy number gain	Abnormal esophagus morphology	GLikely benign