List of variants in gene TNNI3 reported as likely pathogenic 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.484C>T (p.Arg162Trp)	rs368861241	0.00004
NM_000363.5(TNNI3):c.434G>A (p.Arg145Gln)	rs397516349	0.00002
NM_000363.5(TNNI3):c.12-1G>T	rs397516340	0.00001
NM_000363.5(TNNI3):c.485G>A (p.Arg162Gln)	rs397516354	0.00001
NM_000363.5(TNNI3):c.497C>T (p.Ser166Phe)	rs727504242	0.00001
NM_000363.5(TNNI3):c.586G>A (p.Asp196Asn)	rs104894727	0.00001
NM_000363.5(TNNI3):c.1A>G (p.Met1Val)	rs397516341
NM_000363.5(TNNI3):c.431T>C (p.Leu144Pro)	rs121917760
NM_000363.5(TNNI3):c.464T>C (p.Met155Thr)	rs397516352
NM_000363.5(TNNI3):c.485G>C (p.Arg162Pro)	rs397516354
NM_000363.5(TNNI3):c.508C>T (p.Arg170Trp)	rs727503504
NM_000363.5(TNNI3):c.550G>A (p.Glu184Lys)	rs397516356
NM_000363.5(TNNI3):c.568G>T (p.Asp190Tyr)	rs727503500
NM_000363.5(TNNI3):c.575G>C (p.Arg192Pro)	rs104894729
NM_000363.5(TNNI3):c.575G>T (p.Arg192Leu)	rs104894729
NM_000363.5(TNNI3):c.602T>C (p.Met201Thr)	rs727504365
NM_000363.5(TNNI3):c.611G>A (p.Arg204His)	rs727504275

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