Related gene-specific medical variations for Gene (Select 6014) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1808951	GRCh37/hg19 18q12.3(chr18:39703214-40584221)x3	RIT2	Copy number gain	not provided	GUncertain significance
Select item 979697	GRCh37/hg19 18q12.3(chr18:40100890-40503349)x3	RIT2	Copy number gain	not provided	GUncertain significance
Select item 816005	GRCh37/hg19 18q12.3(chr18:40548003-40825757)x3	RIT2	Copy number gain	not provided	GUncertain significance
Select item 564493	GRCh37/hg19 18q12.3(chr18:40586824-40806895)x1	RIT2	Copy number loss	not provided	GUncertain significance

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