List of variants in gene combination LOC126806420, TTN reported as likely benign by CHEO Genetics Diagnostic Laboratory, Children's Hospital of Eastern Ontario

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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: 6

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HGVS	dbSNP	gnomAD frequency
NM_001267550.2(TTN):c.99969C>T (p.Ile33323=)	rs375403439	0.00016
NM_001267550.2(TTN):c.99661A>G (p.Ile33221Val)	rs938263270	0.00003
NM_001267550.2(TTN):c.99734T>C (p.Ile33245Thr)	rs749517808	0.00003
NM_001267550.2(TTN):c.99793G>A (p.Ala33265Thr)	rs2468671289
NM_001267550.2(TTN):c.99793_99794delinsAG (p.Ala33265Ser)	rs2468671221
NM_001267550.2(TTN):c.99794C>G (p.Ala33265Gly)	rs2468671150

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