List of variants in gene combination LOC126806430, TTN reported as likely benign by PreventionGenetics, part of Exact Sciences

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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: 7

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HGVS	dbSNP	gnomAD frequency
NM_001267550.2(TTN):c.18325A>G (p.Lys6109Glu)	rs73973139	0.00096
NM_001267550.2(TTN):c.18407G>A (p.Arg6136Gln)	rs117551279	0.00016
NM_001267550.2(TTN):c.18379T>G (p.Cys6127Gly)	rs370812788	0.00011
NM_001267550.2(TTN):c.18561G>A (p.Ala6187=)	rs377556808	0.00004
NM_001267550.2(TTN):c.18942C>T (p.Thr6314=)	rs572285982	0.00004
NM_001267550.2(TTN):c.18363G>A (p.Gln6121=)	rs375032616	0.00003
NM_001267550.2(TTN):c.18645C>T (p.Asp6215=)	rs372400829	0.00003

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