List of variants in gene combination LOC126806422, TTN reported as likely benign by Diagnostic Laboratory, Department of Genetics, University Medical Center Groningen

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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.69585C>T (p.Ser23195=)	rs67041405	0.01183
NM_001267550.2(TTN):c.69740C>T (p.Pro23247Leu)	rs115658240	0.00835
NM_001267550.2(TTN):c.69676A>G (p.Ser23226Gly)	rs72646885	0.00553
NM_001267550.2(TTN):c.69716-5C>G	rs72646886	0.00290
NM_001267550.2(TTN):c.69821G>A (p.Gly23274Asp)	rs201043950	0.00110
NM_001267550.2(TTN):c.70097T>C (p.Val23366Ala)	rs372782502	0.00030
NM_001267550.2(TTN):c.70644C>T (p.Thr23548=)	rs148210834	0.00019
NM_001267550.2(TTN):c.70651C>T (p.Leu23551=)	rs72646889	0.00011
NM_001267550.2(TTN):c.69630C>T (p.Tyr23210=)	rs777602537	0.00001

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