Related gene-specific medical variations for Gene (Select 835) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3137593	NM_032982.4(CASP2):c.71G>T (p.Arg24Leu)	CASP2, LOC129999515 (R24L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3057249	NM_032982.4(CASP2):c.55G>A (p.Ala19Thr)	CASP2, LOC129999515 (A19T)	Single nucleotide variant (missense variant)	CASP2-related disorder	GLikely benign
Select item 2492289	NM_032982.4(CASP2):c.32C>T (p.Thr11Ile)	CASP2, LOC129999515 (T11I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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