List of variants in gene LOC126806423, TTN studied 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

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 14

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HGVS	dbSNP	gnomAD frequency
NM_001267550.2(TTN):c.67808C>T (p.Ala22603Val)	rs199583938	0.00010
NM_001267550.2(TTN):c.67606G>A (p.Glu22536Lys)	rs371105318	0.00006
NM_001267550.2(TTN):c.68298C>A (p.Asp22766Glu)	rs534340303	0.00005
NM_001267550.2(TTN):c.67495C>T (p.Arg22499Ter)	rs574660186	0.00004
NM_001267550.2(TTN):c.67882G>A (p.Val22628Ile)	rs775731759	0.00004
NM_001267550.2(TTN):c.68007G>A (p.Lys22669=)	rs755897447	0.00004
NM_001267550.2(TTN):c.67487A>G (p.Lys22496Arg)	rs397517669	0.00002
NM_001267550.2(TTN):c.67496G>A (p.Arg22499Gln)	rs767993624	0.00002
NM_001267550.2(TTN):c.67685C>A (p.Ala22562Asp)	rs776797528	0.00002
NM_001267550.2(TTN):c.67792A>C (p.Ser22598Arg)	rs775579156	0.00002
NM_001267550.2(TTN):c.67637-9A>G	rs2047164551	0.00001
NM_001267550.2(TTN):c.68078C>T (p.Thr22693Met)	rs758700425	0.00001
NM_001267550.2(TTN):c.68235T>C (p.Asp22745=)	rs757244505
NM_001267550.2(TTN):c.68308del (p.Thr22770fs)	rs1064796112

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