List of variants in gene combination LOC129935182, 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: 14

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HGVS	dbSNP	gnomAD frequency
NM_001267550.2(TTN):c.106121T>A (p.Phe35374Tyr)	rs727504609	0.00011
NM_001267550.2(TTN):c.106044C>A (p.Asn35348Lys)	rs145560044	0.00006
NM_001267550.2(TTN):c.106020T>C (p.Gly35340=)	rs148865574	0.00003
NM_001267550.2(TTN):c.106134C>A (p.Ala35378=)	rs372562222	0.00003
NM_001267550.2(TTN):c.106083T>C (p.Ile35361=)	rs1196945123	0.00002
NM_001267550.2(TTN):c.106152G>A (p.Glu35384=)	rs776327038	0.00002
NM_001267550.2(TTN):c.106029G>A (p.Glu35343=)	rs985272969	0.00001
NM_001267550.2(TTN):c.106047C>A (p.Leu35349=)	rs768200270	0.00001
NM_001267550.2(TTN):c.106101G>A (p.Thr35367=)	rs754154871	0.00001
NM_001267550.2(TTN):c.106143T>C (p.Ser35381=)	rs961119478	0.00001
NM_001267550.2(TTN):c.106083T>A (p.Ile35361=)
NM_001267550.2(TTN):c.106119A>G (p.Gln35373=)
NM_001267550.2(TTN):c.106128G>T (p.Gly35376=)
NM_001267550.2(TTN):c.106188T>C (p.Asp35396=)	rs770681247

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