List of variants in gene combination LOC126806427, TTN reported as benign for Dilated cardiomyopathy 1G; Autosomal recessive limb-girdle muscular dystrophy type 2J

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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: 11

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HGVS	dbSNP	gnomAD frequency
NM_001267550.2(TTN):c.45526C>T (p.Leu15176=)	rs61004744	0.02387
NM_001267550.2(TTN):c.45206A>T (p.Glu15069Val)	rs114331773	0.01832
NM_001267550.2(TTN):c.45328G>A (p.Asp15110Asn)	rs17354992	0.00698
NM_001267550.2(TTN):c.45083-10A>G	rs72677222	0.00683
NM_001267550.2(TTN):c.45350-13T>C	rs113084617	0.00600
NM_001267550.2(TTN):c.45408G>T (p.Lys15136Asn)	rs72677225	0.00512
NM_001267550.2(TTN):c.45175G>A (p.Ala15059Thr)	rs144668626	0.00104
NM_001267550.2(TTN):c.45174C>T (p.Gly15058=)	rs372609980	0.00079
NM_001267550.2(TTN):c.45599C>G (p.Ala15200Gly)	rs201057307	0.00033
NM_001267550.2(TTN):c.45053C>T (p.Ala15018Val)	rs72677221
NM_001267550.2(TTN):c.45120T>G (p.Ile15040Met)	rs74580375

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