ClinVar Miner

List of variants in gene TNNI3 reported as likely benign by CeGaT Center for Human Genetics Tuebingen

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: 2

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HGVS	dbSNP	gnomAD frequency
NM_000363.5(TNNI3):c.-47C>T	rs202159627	0.00625
NM_000363.5(TNNI3):c.522G>A (p.Lys174=)	rs730880231

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