List of variants in gene KCNN2 reported as pathogenic by Institute for Human Genetics, University Hospital Essen

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_021614.4(KCNN2):c.1116C>A (p.Tyr372Ter)	rs774833524
NM_021614.4(KCNN2):c.1436_1439del (p.Leu478_Tyr479insTer)	rs1758879579
NM_021614.4(KCNN2):c.1598_1600del (p.Leu533del)	rs1554086554

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