Related gene-specific medical variations for Gene (Select 157) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1341202	GRCh37/hg19 22q11.23-12.1(chr22:25656237-26003361)x3	GRK3	Copy number gain	not provided	GLikely benign
Select item 816214	GRCh37/hg19 22q11.23-12.1(chr22:25656220-26120408)x4	GRK3	Copy number gain	not provided	GLikely benign
Select item 157474	Single allele	GRK3	Duplication	Large for gestational age	Gnot provided

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