List of variants in gene combination LOC129935184, TTN reported as likely 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: 9

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HGVS	dbSNP	gnomAD frequency
NM_001267550.2(TTN):c.105505C>T (p.Leu35169=)	rs746050101	0.00004
NM_001267550.2(TTN):c.105512C>T (p.Thr35171Ile)	rs774524898	0.00004
NM_001267550.2(TTN):c.105492T>C (p.Arg35164=)	rs775290030	0.00001
NM_001267550.2(TTN):c.105570A>G (p.Ser35190=)	rs377340289	0.00001
NM_001267550.2(TTN):c.105498A>G (p.Gly35166=)	rs2154133248
NM_001267550.2(TTN):c.105501A>G (p.Gln35167=)
NM_001267550.2(TTN):c.105504G>C (p.Val35168=)
NM_001267550.2(TTN):c.105525C>T (p.His35175=)
NM_001267550.2(TTN):c.105543G>A (p.Lys35181=)	rs1575225685

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