List of variants in gene combination LOC130065089, TNNT1 reported as likely benign for hereditary skeletal muscle disorder

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_003283.6(TNNT1):c.193-11G>A
NM_003283.6(TNNT1):c.193-14C>T
NM_003283.6(TNNT1):c.193-5del
NM_003283.6(TNNT1):c.193-6C>T	rs762393569
NM_003283.6(TNNT1):c.219A>G (p.Lys73=)	rs749449831

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