List of variants in gene combination LOC126806423, TTN reported as likely benign by CeGaT Center for Human Genetics Tuebingen

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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.67833C>T (p.Tyr22611=)	rs375538420	0.00027
NM_001267550.2(TTN):c.68160C>T (p.Ala22720=)	rs397517673	0.00001
NM_001267550.2(TTN):c.68196G>A (p.Ser22732=)	rs397517674	0.00001
NM_001267550.2(TTN):c.67587T>C (p.Asn22529=)	rs1057523544
NM_001267550.2(TTN):c.67740A>G (p.Pro22580=)
NM_001267550.2(TTN):c.67890C>G (p.Gly22630=)

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