C4084841[trait identifier] AND "Genome-Nilou Lab"[submitter] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 126293	NM_024809.5(TCTN2):c.891+22T>C	TCTN2	Single nucleotide variant (intron variant)	Joubert syndrome 24 +3 more	GBenign
Select item 126282	NM_024809.5(TCTN2):c.1099+19T>C	TCTN2	Single nucleotide variant (intron variant)	Joubert syndrome 24 +5 more	GBenign
Select item 126283	NM_024809.5(TCTN2):c.1128T>C (p.Pro376=)	TCTN2	Single nucleotide variant (synonymous variant)	Familial aplasia of the vermis +5 more	GBenign

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