Related gene-specific medical variations for Gene (Select 158219) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 980894	GRCh37/hg19 9p22.3(chr9:14986782-15296450)x1	TTC39B	Copy number loss	not provided	GLikely benign
Select item 815237	GRCh37/hg19 9p22.3(chr9:15230481-15371734)x1	TTC39B	Copy number loss	not provided	GLikely benign
Select item 226198	GRCh37/hg19 9p22.3(chr9:15300542-15381614)	TTC39B	Copy number loss	Abnormal esophagus morphology	GBenign

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