C3280766[trait identifier] AND "Baylor Genetics"[submitter] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 183328	NM_001044385.3(TMEM237):c.869+1G>A	TMEM237	Single nucleotide variant (splice donor variant)	Joubert syndrome 14	GPathogenic/Likely pathogenic
Select item 960602	NM_001044385.3(TMEM237):c.287C>T (p.Ser96Phe)	TMEM237 (S88F +1 more)	Single nucleotide variant (missense variant)	Joubert syndrome 14 +1 more	GUncertain significance
Select item 1033245	NM_001044385.3(TMEM237):c.42+1G>A	TMEM237	Single nucleotide variant (splice donor variant)	not provided +1 more	GConflicting classifications of pathogenicity

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ClinVar