C5542277[trait identifier] AND "Genome-Nilou Lab"[submitter] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 194954	NM_004239.4(TRIP11):c.5479G>A (p.Gly1827Ser)	TRIP11 (G1827S +1 more)	Single nucleotide variant (missense variant)	not specified +3 more	GBenign
Select item 1178934	NM_004239.4(TRIP11):c.5260+24T>C	TRIP11	Single nucleotide variant (intron variant)	Odontochondrodysplasia 1 +2 more	GBenign
Select item 1261817	NM_004239.4(TRIP11):c.1527+41A>G	TRIP11	Single nucleotide variant (intron variant)	Achondrogenesis, type IA +2 more	GBenign

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