C4748014[trait identifier] AND "Clinical Genomics Program, Stanford Me - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1774197	NM_020778.5(ALPK3):c.904C>A (p.Leu302Met)	ALPK3 (L302M)	Single nucleotide variant (missense variant)	not provided +2 more	GUncertain significance
Select item 1503713	NM_020778.5(ALPK3):c.2391C>A (p.Asn797Lys)	ALPK3 (N797K)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 1193213	NM_020778.5(ALPK3):c.3038G>A (p.Arg1013His)	ALPK3 (R1013H)	Single nucleotide variant (missense variant)	Cardiovascular phenotype +2 more	GUncertain significance

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