List of variants in gene combination LOC126806430, 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: 13

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HGVS	dbSNP	gnomAD frequency
NM_001267550.2(TTN):c.18776C>G (p.Thr6259Ser)	rs72648949	0.00262
NM_001267550.2(TTN):c.18659G>C (p.Cys6220Ser)	rs191692293	0.00188
NM_001267550.2(TTN):c.18856G>A (p.Val6286Ile)	rs149131555	0.00184
NM_001267550.2(TTN):c.18961A>G (p.Ile6321Val)	rs145204073	0.00146
NM_001267550.2(TTN):c.18816T>C (p.Ile6272=)	rs146219199	0.00012
NM_001267550.2(TTN):c.18379T>G (p.Cys6127Gly)	rs370812788	0.00011
NM_001267550.2(TTN):c.18307+12A>G	rs376899412	0.00009
NM_001267550.2(TTN):c.18231C>T (p.Thr6077=)	rs377639910	0.00006
NM_001267550.2(TTN):c.18561G>A (p.Ala6187=)	rs377556808	0.00004
NM_001267550.2(TTN):c.18363G>A (p.Gln6121=)	rs375032616	0.00003
NM_001267550.2(TTN):c.18609A>G (p.Arg6203=)	rs777227340	0.00002
NM_001267550.2(TTN):c.18456T>C (p.His6152=)	rs756540833	0.00001
NM_001267550.2(TTN):c.18810G>A (p.Gln6270=)	rs727505012

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