List of variants in gene combination LOC126806429, 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: 5

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HGVS	dbSNP	gnomAD frequency
NM_001267550.2(TTN):c.19745G>A (p.Arg6582Gln)	rs776051087	0.00005
NM_001267550.2(TTN):c.19922C>A (p.Thr6641Asn)	rs747240394	0.00003
NM_001267550.2(TTN):c.19949A>G (p.Asn6650Ser)	rs751222632	0.00001
NM_001267550.2(TTN):c.19890C>G (p.Phe6630Leu)	rs2529810138
NM_001267550.2(TTN):c.19940A>G (p.His6647Arg)	rs757799209

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