List of variants in gene TNNT3 reported as benign for Sheldon-hall syndrome

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: 12

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HGVS	dbSNP	gnomAD frequency
NM_006757.4(TNNT3):c.83-48A>G	rs629990	0.81000
NM_006757.4(TNNT3):c.107-115T>C	rs2292471	0.80994
NM_006757.4(TNNT3):c.681+63T>C	rs513735	0.79566
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.762C>T (p.Gly254=)	rs4727	0.12344
NM_006757.4(TNNT3):c.636T>C (p.Ile212=)	rs16927166	0.03978
NM_006757.4(TNNT3):c.367-9T>C	rs76471485	0.00859
NM_006757.4(TNNT3):c.*36C>T	rs147535560	0.00188
NM_006757.4(TNNT3):c.480+10G>T	rs188255267	0.00143
NM_006757.4(TNNT3):c.*86C>T	rs200540491	0.00003
NM_006757.4(TNNT3):c.107-134T>G	rs2292473

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