List of variants in gene combination LOC126806420, 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: 9

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HGVS	dbSNP	gnomAD frequency
NM_001267550.2(TTN):c.100096G>A (p.Val33366Ile)	rs55675869	0.02155
NM_001267550.2(TTN):c.100094G>A (p.Arg33365Gln)	rs55742743	0.01280
NM_001267550.2(TTN):c.99901G>A (p.Glu33301Lys)	rs72648278	0.00038
NM_001267550.2(TTN):c.99866-10C>T	rs773128928	0.00029
NM_001267550.2(TTN):c.100284C>T (p.Tyr33428=)	rs1440086089	0.00003
NM_001267550.2(TTN):c.100020A>G (p.Gln33340=)	rs375614764	0.00001
NM_001267550.2(TTN):c.99900C>T (p.Ile33300=)	rs747130957	0.00001
NM_001267550.2(TTN):c.99927G>C (p.Val33309=)	rs752424641	0.00001
NM_001267550.2(TTN):c.100119C>T (p.Gly33373=)	rs2468650757

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