Related gene-specific medical variations for Gene (Select 57482) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3077117	NM_001393381.1(CRACD):c.296C>T (p.Thr99Met)	CRACD, LOC126807059 (T99M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1527089	GRCh37/hg19 4q12(chr4:56946533-57046730)	CRACD	Copy number loss	not specified	GUncertain significance
Select item 814557	GRCh37/hg19 4q12(chr4:56942915-57151080)x1	CRACD	Copy number loss	not provided	GUncertain significance

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