List of variants in gene combination LOC126806430, 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: 8

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HGVS	dbSNP	gnomAD frequency
NM_001267550.2(TTN):c.18659G>C (p.Cys6220Ser)	rs191692293	0.00188
NM_001267550.2(TTN):c.18824A>G (p.Asn6275Ser)	rs184412722	0.00111
NM_001267550.2(TTN):c.18325A>G (p.Lys6109Glu)	rs73973139	0.00096
NM_001267550.2(TTN):c.18531G>C (p.Val6177=)	rs370684491	0.00088
NM_001267550.2(TTN):c.18172C>T (p.Arg6058Cys)	rs189127014	0.00053
NM_001267550.2(TTN):c.18550G>A (p.Ala6184Thr)	rs72648947	0.00046
NM_001267550.2(TTN):c.18379T>G (p.Cys6127Gly)	rs370812788	0.00011
NM_001267550.2(TTN):c.18303A>T (p.Val6101=)

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