"KCNK9-related disorder"[Disease/phenotype] AND "PreventionGenetics, p - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2628439	NM_001282534.2(KCNK9):c.863C>T (p.Ala288Val)	KCNK9 (A288V)	Single nucleotide variant (missense variant +1 more)	KCNK9-related disorder	GUncertain significance
Select item 720392	NM_001282534.2(KCNK9):c.825C>T (p.Ile275=)	KCNK9	Single nucleotide variant (synonymous variant +1 more)	KCNK9-related disorder +1 more	GBenign/Likely benign
Select item 3040050	NM_001282534.2(KCNK9):c.582C>T (p.Phe194=)	KCNK9	Single nucleotide variant (synonymous variant +1 more)	KCNK9-related disorder	GLikely benign
Select item 3043621	NM_001282534.2(KCNK9):c.459C>T (p.Asp153=)	KCNK9	Single nucleotide variant (synonymous variant +1 more)	KCNK9-related disorder	GLikely benign
Select item 710440	NM_001282534.2(KCNK9):c.375C>T (p.Phe125=)	KCNK9	Single nucleotide variant (synonymous variant +1 more)	KCNK9-related disorder +1 more	GBenign/Likely benign
Select item 709458	NM_001282534.2(KCNK9):c.284-10C>G	KCNK9	Single nucleotide variant (intron variant)	not provided +1 more	GBenign

ClinVar