List of variants in gene combination LOC126806421, TTN reported as uncertain significance for Dilated cardiomyopathy 1G; Autosomal recessive limb-girdle muscular dystrophy type 2J; Tibial muscular dystrophy; Myopathy, myofibrillar, 9, with early respiratory failure; Early-onset myopathy with fatal cardiomyopathy; Hypertrophic cardiomyopathy 9

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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: 11

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HGVS	dbSNP	gnomAD frequency
NM_001267550.2(TTN):c.96928A>C (p.Thr32310Pro)	rs542208825	0.00018
NM_001267550.2(TTN):c.96424G>A (p.Val32142Ile)	rs779663332	0.00006
NM_001267550.2(TTN):c.96637G>A (p.Asp32213Asn)	rs764561909	0.00006
NM_001267550.2(TTN):c.96286G>A (p.Ala32096Thr)	rs376039623	0.00005
NM_001267550.2(TTN):c.96140C>T (p.Thr32047Met)	rs375640847	0.00004
NM_001267550.2(TTN):c.96198C>G (p.Ser32066Arg)	rs747323263	0.00003
NM_001267550.2(TTN):c.96434G>A (p.Arg32145His)	rs759948951	0.00003
NM_001267550.2(TTN):c.96644C>G (p.Thr32215Ser)	rs975713554	0.00003
NM_001267550.2(TTN):c.96934C>T (p.Pro32312Ser)	rs1024823449	0.00003
NM_001267550.2(TTN):c.96698G>A (p.Arg32233Gln)	rs755082341	0.00001
NM_001267550.2(TTN):c.96506T>C (p.Leu32169Pro)	rs2154143527

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