C1849718[trait identifier] AND "Baylor Genetics"[submitter] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1033541	NM_020639.3(RIPK4):c.1511A>G (p.Gln504Arg)	RIPK4 (Q504R)	Single nucleotide variant (missense variant)	Bartsocas-Papas syndrome 1	GUncertain significance
Select item 561098	NM_020639.3(RIPK4):c.488G>A (p.Gly163Asp)	RIPK4 (G163D)	Single nucleotide variant (missense variant)	Bartsocas-Papas syndrome 1	GUncertain significance
Select item 895414	NM_020639.3(RIPK4):c.277G>A (p.Gly93Ser)	RIPK4 (G93S)	Single nucleotide variant (missense variant)	Inborn genetic diseases +1 more	GUncertain significance

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ClinVar