List of variants in gene TTN reported as benign for Primary dilated cardiomyopathy

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 24

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HGVS	dbSNP	gnomAD frequency
NM_001267550.2(TTN):c.2765G>A (p.Arg922His)	rs56046320	0.00295
NM_001267550.2(TTN):c.92537T>C (p.Val30846Ala)	rs77968867	0.00262
NM_001267550.2(TTN):c.64762G>A (p.Gly21588Arg)	rs181717727	0.00261
NM_001267550.2(TTN):c.88708A>G (p.Ile29570Val)	rs139506970	0.00255
NM_001267550.2(TTN):c.97490T>C (p.Ile32497Thr)	rs55660660	0.00251
NM_001267550.2(TTN):c.83740A>G (p.Thr27914Ala)	rs188370772	0.00250
NM_001267550.2(TTN):c.34566A>C (p.Glu11522Asp)	rs140640738	0.00113
NM_001267550.2(TTN):c.90536G>A (p.Arg30179His)	rs149567378	0.00113
NM_001267550.2(TTN):c.13859G>A (p.Gly4620Asp)	rs55857742	0.00111
NM_001267550.2(TTN):c.49919G>C (p.Ser16640Thr)	rs55663050	0.00110
NM_001267550.2(TTN):c.91765G>A (p.Ala30589Thr)	rs148617456	0.00108
NM_001267550.2(TTN):c.95297C>T (p.Ser31766Phe)	rs191484894	0.00108
NM_001267550.2(TTN):c.64789G>A (p.Val21597Met)	rs150661999	0.00107
NM_001267550.2(TTN):c.101891G>A (p.Arg33964His)	rs55669553	0.00106
NM_001267550.2(TTN):c.25490G>A (p.Arg8497His)	rs149855485	0.00106
NM_001267550.2(TTN):c.47545C>A (p.Pro15849Thr)	rs146181477	0.00106
NM_001267550.2(TTN):c.82560C>A (p.Asn27520Lys)	rs56264840	0.00104
NM_001267550.2(TTN):c.90826T>G (p.Cys30276Gly)	rs150430592	0.00103
NM_001267550.2(TTN):c.102595A>G (p.Ile34199Val)	rs56347248	0.00102
NM_001267550.2(TTN):c.80701A>G (p.Ile26901Val)	rs201562505	0.00102
NM_001267550.2(TTN):c.13976A>G (p.Tyr4659Cys)	rs34706803	0.00081
NM_001267550.2(TTN):c.102103G>A (p.Asp34035Asn)	rs144963736	0.00078
NM_001267550.2(TTN):c.23538C>G (p.Phe7846Leu)	rs149523263
NM_001267550.2(TTN):c.60490G>C (p.Val20164Leu)	rs72646843

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