List of variants in gene combination LOC101927055, TTN reported as likely benign for Dilated cardiomyopathy 1G

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
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Total variants: 8

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HGVS	dbSNP	gnomAD frequency
NM_001267550.2(TTN):c.4246C>T (p.Arg1416Cys)	rs72647875	0.01559
NM_001267550.2(TTN):c.3993C>T (p.Ile1331=)	rs55757622	0.01419
NM_001267550.2(TTN):c.4630A>G (p.Ile1544Val)	rs72647877	0.01259
NM_001267550.2(TTN):c.4034G>A (p.Gly1345Asp)	rs36021856	0.01079
NM_001267550.2(TTN):c.4347A>G (p.Ser1449=)	rs719202	0.01042
NM_001267550.2(TTN):c.4739C>T (p.Thr1580Met)	rs73973147	0.00558
NM_001267550.2(TTN):c.4328T>C (p.Leu1443Pro)	rs142317580	0.00188
NM_001267550.2(TTN):c.4322G>C (p.Arg1441Pro)	rs72647876

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