Variants in gene combination LOC126806424, TTN with conflicting interpretations reported as "uncertain significance and "likely benign"

Submission 1 (uncertain significance) minimum review status:		Submission 1 (uncertain significance) method:
Submission 2 (likely benign) minimum review status:		Submission 2 (likely benign) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 20

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HGVS	dbSNP	gnomAD frequency
NM_001267550.2(TTN):c.59318A>G (p.Glu19773Gly)	rs371719028	0.00083
NM_001267550.2(TTN):c.59316G>A (p.Pro19772=)	rs377180286	0.00064
NM_001267550.2(TTN):c.60005A>G (p.Asp20002Gly)	rs199512049	0.00031
NM_001267550.2(TTN):c.59344+3G>A	rs142095604	0.00023
NM_001267550.2(TTN):c.59402G>A (p.Gly19801Asp)	rs202206216	0.00012
NM_001267550.2(TTN):c.59729C>T (p.Thr19910Ile)	rs369476725	0.00010
NM_001267550.2(TTN):c.59849G>A (p.Arg19950Gln)	rs374914334	0.00009
NM_001267550.2(TTN):c.60146G>A (p.Arg20049His)	rs200455644	0.00009
NM_001267550.2(TTN):c.59474G>C (p.Arg19825Thr)	rs376465623	0.00006
NM_001267550.2(TTN):c.60025A>G (p.Ile20009Val)	rs371988490	0.00006
NM_001267550.2(TTN):c.59657T>G (p.Val19886Gly)	rs755949982	0.00005
NM_001267550.2(TTN):c.59926C>T (p.His19976Tyr)	rs727503588	0.00005
NM_001267550.2(TTN):c.60205T>C (p.Cys20069Arg)	rs771201679	0.00004
NM_001267550.2(TTN):c.60008G>A (p.Arg20003His)	rs756091180	0.00003
NM_001267550.2(TTN):c.59534G>A (p.Arg19845His)	rs201457934	0.00002
NM_001267550.2(TTN):c.59937G>A (p.Gly19979=)	rs727505101	0.00002
NM_001267550.2(TTN):c.59502T>C (p.Asp19834=)	rs972823319	0.00001
NM_001267550.2(TTN):c.59812G>A (p.Ala19938Thr)	rs755204306	0.00001
NM_001267550.2(TTN):c.59442A>G (p.Pro19814=)	rs1304742332
NM_001267550.2(TTN):c.59965G>A (p.Val19989Ile)	rs1021499065

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