C2676770[trait identifier] AND "Illumina Laboratory Services, Illumina - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 4741	NM_001282534.2(KCNK9):c.706G>A (p.Gly236Arg)	KCNK9 (G236R)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GPathogenic
Select item 989376	NM_001282534.2(KCNK9):c.599T>C (p.Ile200Thr)	KCNK9 (I200T)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GUncertain significance
Select item 372887	NM_001282534.2(KCNK9):c.392G>A (p.Arg131His)	KCNK9 (R131H)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases +2 more	GLikely pathogenic

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ClinVar