List of variants in gene combination LOC126806423, TTN reported as likely benign by Women's Health and Genetics/Laboratory Corporation of America, LabCorp

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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: 5

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HGVS	dbSNP	gnomAD frequency
NM_001267550.2(TTN):c.68082C>T (p.Cys22694=)	rs79406408	0.00024
NM_001267550.2(TTN):c.67959T>C (p.Phe22653=)	rs72646877	0.00016
NM_001267550.2(TTN):c.68165A>G (p.Asn22722Ser)	rs200493270	0.00010
NM_001267550.2(TTN):c.67681T>C (p.Leu22561=)	rs397517671	0.00001
NM_001267550.2(TTN):c.68225-18T>C	rs1416277306

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