C5193097[trait identifier] AND "Genome-Nilou Lab"[submitter] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 31868	NM_006757.4(TNNT3):c.18-76A>G	TNNT3	Single nucleotide variant (intron variant)	Arthrogryposis, distal, type 2B2 +1 more	GBenign
Select item 31869	NM_006757.4(TNNT3):c.32-149A>T	TNNT3	Single nucleotide variant (intron variant)	Arthrogryposis, distal, type 2B2 +1 more	GBenign
Select item 260032	NM_006757.4(TNNT3):c.83-48A>G	TNNT3	Single nucleotide variant (intron variant)	not provided +2 more	GBenign
Select item 1185427	NM_006757.4(TNNT3):c.107-134T>G	TNNT3	Single nucleotide variant (intron variant)	Arthrogryposis, distal, type 2B2 +1 more	GBenign
Select item 1185428	NM_006757.4(TNNT3):c.107-115T>C	TNNT3	Single nucleotide variant (intron variant)	not provided +1 more	GBenign
Select item 1185429	NM_006757.4(TNNT3):c.681+63T>C	TNNT3	Single nucleotide variant (intron variant)	Arthrogryposis, distal, type 2B2 +1 more	GBenign

ClinVar