List of variants in gene combination LOC126806429, TTN reported as likely benign by Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 9

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HGVS	dbSNP	gnomAD frequency
NM_001267550.2(TTN):c.19738C>T (p.Pro6580Ser)	rs116572520	0.00188
NM_001267550.2(TTN):c.20236G>A (p.Ala6746Thr)	rs202108224	0.00081
NM_001267550.2(TTN):c.19728C>T (p.Phe6576=)	rs751902051	0.00003
NM_001267550.2(TTN):c.19818A>G (p.Lys6606=)	rs397517492	0.00003
NM_001267550.2(TTN):c.19922C>A (p.Thr6641Asn)	rs747240394	0.00003
NM_001267550.2(TTN):c.20169C>T (p.Ala6723=)	rs727504776	0.00001
NM_001267550.2(TTN):c.19914T>C (p.Ala6638=)	rs1317197263
NM_001267550.2(TTN):c.20142C>T (p.Tyr6714=)	rs535793314
NM_001267550.2(TTN):c.20263G>C (p.Val6755Leu)	rs876657599

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