List of variants in gene TNNT3 reported as not provided

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: 10

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HGVS	dbSNP	gnomAD frequency
NM_006757.4(TNNT3):c.32-149A>T	rs2734500	0.76033
NM_006757.4(TNNT3):c.18-76A>G	rs965912	0.73230
NM_006757.4(TNNT3):c.-18-482G>A	rs1398256	0.73144
NM_006757.4(TNNT3):c.762C>T (p.Gly254=)	rs4727	0.12344
NM_006757.4(TNNT3):c.636T>C (p.Ile212=)	rs16927166	0.03978
NM_006757.4(TNNT3):c.414G>A (p.Glu138=)	rs2292470	0.00576
NM_006757.4(TNNT3):c.328C>T (p.Arg110Cys)	rs144957238	0.00009
NM_006757.4(TNNT3):c.-18-379C>A	rs2334385
NM_006757.4(TNNT3):c.187C>T (p.Arg63Cys)	rs199474721
NM_006757.4(TNNT3):c.188G>A (p.Arg63His)	rs121434638

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