"GeneReviews"[submitter] AND "KCNJ2"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 8923	NM_000891.3(KCNJ2):c.199C>T (p.Arg67Trp)	KCNJ2	Single nucleotide variant (missense variant)	Atrial fibrillation, familial, 9 +5 more	GPathogenic
Select item 208080	NM_000891.3(KCNJ2):c.271_282del (p.Ala91_Leu94del)	KCNJ2	Deletion (inframe_deletion)	Andersen Tawil syndrome	Gnot provided
Select item 8919	NM_000891.3(KCNJ2):c.652C>T (p.Arg218Trp)	KCNJ2	Single nucleotide variant (missense variant)	Andersen Tawil syndrome +3 more	GPathogenic/Likely pathogenic
Select item 546134	NM_000891.3(KCNJ2):c.665T>C (p.Leu222Ser)	KCNJ2 (L222S)	Single nucleotide variant (missense variant)	not provided	GLikely pathogenic
Select item 67588	NM_000891.3(KCNJ2):c.899G>A (p.Gly300Asp)	KCNJ2	Single nucleotide variant (missense variant)	not provided +2 more	GPathogenic
Select item 161257	NM_000891.3(KCNJ2):c.953A>G (p.Asn318Ser)	KCNJ2	Single nucleotide variant (missense variant)	Andersen Tawil syndrome +4 more	GUncertain significance
Select item 208081	NM_000891.3(KCNJ2):c.966G>C (p.Trp322Cys)	KCNJ2	Single nucleotide variant (missense variant)	Andersen Tawil syndrome	Gnot provided

ClinVar