List of variants in gene KCNJ2 reported as likely benign for Andersen Tawil syndrome

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.1229A>G (p.Asn410Ser)	rs141069645	0.00042
NM_000891.3(KCNJ2):c.-2C>T	rs144760658	0.00013
NM_000891.3(KCNJ2):c.867C>T (p.Asn289=)	rs201909993	0.00010

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