Related gene-specific medical variations for Gene (Select 3782) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2639378	NM_002249.6(KCNN3):c.1449-3920T>G	KCNN3, LOC126805875	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 2433011	NM_002249.6(KCNN3):c.2059C>T (p.Gln687Ter)	KCNN3 (Q374* +4 more)	Single nucleotide variant (nonsense)	Zimmermann-laband syndrome 3	GUncertain significance
Select item 1679705	NM_002249.6(KCNN3):c.1701+3059C>T	KCNN3	Single nucleotide variant (intron variant)	Zimmermann-laband syndrome 3	GUncertain significance
Select item 1098591	NM_002249.6(KCNN3):c.2080G>A (p.Glu694Lys)	KCNN3 (E381K +4 more)	Single nucleotide variant (missense variant)	Zimmermann-laband syndrome 3	GUncertain significance
Select item 161592	NM_002249.6(KCNN3):c.1448+1G>T	KCNN3	Single nucleotide variant (splice donor variant)	Malignant tumor of prostate	GUncertain significance

ClinVar