List of variants in gene TNNT3 reported as likely benign for congenital limb malformation

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_006757.4(TNNT3):c.367-9T>C	rs76471485	0.00859
NM_006757.3(TNNT3):c.-83G>A	rs114407235	0.00585
NM_006757.4(TNNT3):c.414G>A (p.Glu138=)	rs2292470	0.00576
NM_006757.4(TNNT3):c.723-15G>C	rs143255528	0.00407
NM_006757.4(TNNT3):c.*36C>T	rs147535560	0.00188

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