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

Submission 1 (uncertain significance) minimum review status:		Submission 1 (uncertain significance) method:
Submission 2 (benign) minimum review status:		Submission 2 (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: 3

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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.60005A>G (p.Asp20002Gly)	rs199512049	0.00031
NM_001267550.2(TTN):c.59344+3G>A	rs142095604	0.00023

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