List of variants in gene TNNT1 reported as benign for hereditary skeletal muscle disorder

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: 14

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HGVS	dbSNP	gnomAD frequency
NM_003283.6(TNNT1):c.795= (p.Arg265=)	rs890868	0.99361
NM_003283.6(TNNT1):c.47-13C>T	rs11669534	0.11553
NM_003283.6(TNNT1):c.129-9T>G	rs67795913	0.10318
NM_003283.6(TNNT1):c.751-16T>C	rs77273500	0.03649
NM_003283.6(TNNT1):c.795G>T (p.Arg265=)	rs890868	0.00639
NM_003283.6(TNNT1):c.310-14T>C	rs115663668	0.00636
NM_003283.6(TNNT1):c.279A>G (p.Glu93=)	rs34313388	0.00292
NM_003283.6(TNNT1):c.780C>T (p.His260=)	rs78810486	0.00121
NM_003283.6(TNNT1):c.107-16C>A	rs187180704	0.00056
NM_003283.6(TNNT1):c.791+12C>T	rs201143291	0.00006
NM_003283.6(TNNT1):c.502-17G>A	rs370760520	0.00004
NM_003283.6(TNNT1):c.502-9dup
NM_003283.6(TNNT1):c.74-8dup	rs1156241533
NM_003283.6(TNNT1):c.751-5C>T	rs192248377

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