List of variants in gene combination LOC126806425, 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: 6

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HGVS	dbSNP	gnomAD frequency
NM_001267550.2(TTN):c.52852C>T (p.Arg17618Cys)	rs201213901	0.00115
NM_001267550.2(TTN):c.52536C>G (p.Asn17512Lys)	rs199615557	0.00034
NM_001267550.2(TTN):c.52788T>A (p.Asn17596Lys)	rs375966756	0.00002
NM_001267550.2(TTN):c.52667G>A (p.Ser17556Asn)	rs750715335	0.00001
NM_001267550.2(TTN):c.52948G>A (p.Ala17650Thr)	rs535008556	0.00001
NM_001267550.2(TTN):c.53122_53123delinsGT (p.Lys17708Val)	rs886042743

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