rs104894246[Variant ID] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1055539	NM_153766.3(KCNJ1):c.584C>G (p.Ala195Gly)	KCNJ1 (A195G +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 9157	NM_153766.3(KCNJ1):c.584C>T (p.Ala195Val)	KCNJ1 (A195V +2 more)	Single nucleotide variant (missense variant)	not provided +1 more	GPathogenic/Likely pathogenic