List of variants in gene combination LOC126806431, TTN reported as likely benign for Cardiomyopathy

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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: 7

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HGVS	dbSNP	gnomAD frequency
NM_001267550.2(TTN):c.16863G>A (p.Glu5621=)	rs727504441	0.00003
NM_001267550.2(TTN):c.17207T>C (p.Ile5736Thr)	rs1473469854	0.00002
NM_001267550.2(TTN):c.16790C>T (p.Ser5597Phe)	rs754116386	0.00001
NM_001267550.2(TTN):c.17075T>C (p.Val5692Ala)	rs570039271	0.00001
NM_001267550.2(TTN):c.17320G>A (p.Asp5774Asn)	rs752660722	0.00001
NM_001267550.2(TTN):c.17068C>T (p.His5690Tyr)	rs2154309624
NM_001267550.2(TTN):c.17182+10G>C	rs2080543923

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