List of variants in gene combination LOC129935183, TTN reported as benign for Early-onset myopathy with fatal cardiomyopathy

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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: 6

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HGVS	dbSNP	gnomAD frequency
NM_001267550.2(TTN):c.105582C>T (p.Ser35194=)	rs3829749	0.05620
NM_001267550.2(TTN):c.105782C>T (p.Pro35261Leu)	rs16866380	0.04073
NM_001267550.2(TTN):c.105769G>A (p.Glu35257Lys)	rs56324595	0.01324
NM_001267550.2(TTN):c.105787G>T (p.Ala35263Ser)	rs67254537	0.01037
NM_001267550.2(TTN):c.105788C>T (p.Ala35263Val)	rs66961115	0.01037
NM_001267550.2(TTN):c.105787_105788delinsTT (p.Ala35263Phe)	rs794729250

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