List of variants in gene TTN reported as likely benign by Institute of Human Genetics, University of Wuerzburg

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_001267550.2(TTN):c.1492G>A (p.Val498Ile)	rs72647851	0.01678
NM_001267550.2(TTN):c.81558T>C (p.Asn27186=)	rs56181243	0.00615
NM_001267550.2(TTN):c.12580A>T (p.Ile4194Phe)	rs34618570	0.00613

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