List of variants in gene TNNI3 reported as likely benign by Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine

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: 17

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HGVS	dbSNP	gnomAD frequency
NM_000363.5(TNNI3):c.550-10C>T	rs201240150	0.00190
NM_000363.5(TNNI3):c.373-15C>G	rs192630178	0.00141
NM_000363.5(TNNI3):c.25-4C>T	rs202086705	0.00069
NM_000363.5(TNNI3):c.132G>C (p.Ser44=)	rs727504941	0.00012
NM_000363.5(TNNI3):c.246G>T (p.Pro82=)	rs397516343	0.00007
NM_000363.5(TNNI3):c.373-4C>G	rs2288530	0.00007
NM_000363.5(TNNI3):c.39C>G (p.Arg13=)	rs397516346	0.00005
NM_000363.5(TNNI3):c.303C>T (p.His101=)	rs199539066	0.00004
NM_000363.5(TNNI3):c.372+7C>T	rs367809676	0.00004
NM_000363.5(TNNI3):c.6G>A (p.Ala2=)	rs397516361	0.00004
NM_000363.5(TNNI3):c.304G>A (p.Ala102Thr)	rs374618872	0.00003
NM_000363.5(TNNI3):c.258C>T (p.Ala86=)	rs727503508	0.00001
NM_000363.5(TNNI3):c.336C>T (p.Tyr112=)	rs559450042	0.00001
NM_000363.5(TNNI3):c.384G>A (p.Leu128=)	rs373130533	0.00001
NM_000363.5(TNNI3):c.105C>A (p.Ala35=)	rs397516339
NM_000363.5(TNNI3):c.12-7del	rs370714315
NM_000363.5(TNNI3):c.150+13G>T	rs73617692

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