Related gene-specific medical variations for Gene (Select 27033) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3191987	NM_014383.3(ZBTB32):c.121C>G (p.Pro41Ala)	LOC130064255, ZBTB32 (P41A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2293204	NM_014383.3(ZBTB32):c.178T>C (p.Trp60Arg)	LOC130064255, ZBTB32 (W60R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance