ClinVar Miner

List of variants in gene TNNI3 reported as likely benign by CeGaT Praxis fuer Humangenetik 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
NM_000363.5(TNNI3):c.303C>T (p.His101=)	rs199539066
NM_000363.5(TNNI3):c.384G>A (p.Leu128=)	rs373130533

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