"OMIM"[submitter] AND "KCNJ8"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 157543	NM_004982.4(KCNJ8):c.1265C>T (p.Ser422Leu)	KCNJ8 (S422L)	Single nucleotide variant (missense variant)	KCNJ8-related condition +4 more	GBenign/Likely benign
Select item 157545	NM_004982.4(KCNJ8):c.526T>A (p.Cys176Ser)	KCNJ8 (C176S)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 157544	NM_004982.4(KCNJ8):c.193G>A (p.Val65Met)	KCNJ8 (V65M)	Single nucleotide variant (missense variant)	not provided	GUncertain significance

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