Related gene-specific medical variations for Gene (Select 60598) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2559796	NM_022358.4(KCNK15):c.244G>A (p.Gly82Ser)	KCNK15, KCNK15-AS1 (G82S)	Single nucleotide variant (non-coding transcript variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2530176	NM_022358.4(KCNK15):c.105C>A (p.Ser35Arg)	KCNK15, KCNK15-AS1 (S35R)	Single nucleotide variant (non-coding transcript variant +1 more)	Inborn genetic diseases	GLikely benign