C1563715[trait identifier] AND "Centre for Mendelian Genomics, Univers - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 932125	NM_000891.3(KCNJ2):c.578T>C (p.Leu193Pro)	KCNJ2 (L193P)	Single nucleotide variant (missense variant)	Andersen Tawil syndrome +1 more	GConflicting classifications of pathogenicity
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