List of variants in gene KCNJ2 reported as pathogenic by Clinical Molecular Genetics Laboratory, Johns Hopkins All Children's Hospital

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_000891.3(KCNJ2):c.200G>A (p.Arg67Gln)	rs199473368
NM_000891.3(KCNJ2):c.244C>T (p.Arg82Trp)	rs199473373
NM_000891.3(KCNJ2):c.913A>G (p.Thr305Ala)	rs199473387

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