List of variants in gene combination LOC101927055, TTN reported as likely benign by Genetic Services Laboratory, University of Chicago

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_001267550.2(TTN):c.4177A>G (p.Ile1393Val)	rs16866531	0.03468
NM_001267550.2(TTN):c.4246C>T (p.Arg1416Cys)	rs72647875	0.01559
NM_001267550.2(TTN):c.4328T>C (p.Leu1443Pro)	rs142317580	0.00188
NM_001267550.2(TTN):c.4322G>C (p.Arg1441Pro)	rs72647876

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