List of variants in gene KCNN4 reported as pathogenic for hematologic disorder

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_002250.3(KCNN4):c.1055G>A (p.Arg352His)	rs774455945
NM_002250.3(KCNN4):c.844G>A (p.Val282Met)	rs1057519076
NM_002250.3(KCNN4):c.845T>A (p.Val282Glu)	rs1057519077
NM_002250.3(KCNN4):c.940T>C (p.Ser314Pro)	rs1969582489

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