List of variants in gene TTN reported as uncertain significance by Clinical Molecular Genetics Laboratory, Johns Hopkins All Children's Hospital

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.27485C>T (p.Thr9162Met)	rs199793620	0.00034
NM_001267550.2(TTN):c.81302G>T (p.Gly27101Val)	rs201490050	0.00032
NM_001267550.2(TTN):c.93244G>A (p.Glu31082Lys)	rs199663613	0.00020
NM_001267550.2(TTN):c.76566_76568dup (p.Arg25523dup)	rs772268958	0.00006

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