List of variants in gene combination LOC126806427, 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)
		ClinVar version:

Total variants: 8

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HGVS	dbSNP	gnomAD frequency
NM_001267550.2(TTN):c.45526C>T (p.Leu15176=)	rs61004744	0.02213
NM_001267550.2(TTN):c.45206A>T (p.Glu15069Val)	rs114331773	0.01832
NM_001267550.2(TTN):c.45083-10A>G	rs72677222	0.00656
NM_001267550.2(TTN):c.45350-13T>C	rs113084617	0.00600
NM_001267550.2(TTN):c.45175G>A (p.Ala15059Thr)	rs144668626	0.00161
NM_001267550.2(TTN):c.45174C>T (p.Gly15058=)	rs372609980	0.00079
NM_001267550.2(TTN):c.45053C>T (p.Ala15018Val)	rs72677221
NM_001267550.2(TTN):c.45120T>G (p.Ile15040Met)	rs74580375

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