List of variants in gene combination LOC126806430, TTN reported as uncertain significance by Mayo Clinic Laboratories, Mayo Clinic

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.18550G>A (p.Ala6184Thr)	rs72648947	0.00046
NM_001267550.2(TTN):c.18893T>C (p.Ile6298Thr)	rs375571785	0.00006
NM_001267550.2(TTN):c.18781T>A (p.Cys6261Ser)

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