Variants in gene combination LOC101927055, TTN with conflicting interpretations reported as "likely pathogenic and "uncertain significance"

Submission 1 (likely pathogenic) minimum review status:		Submission 1 (likely pathogenic) method:
Submission 2 (uncertain significance) minimum review status:		Submission 2 (uncertain significance) 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.3742_3745del (p.Ser1248fs)	rs2154347788
NM_001267550.2(TTN):c.4714C>T (p.Arg1572Ter)	rs1554008881
NM_001267550.2(TTN):c.4724_4728del (p.Met1575fs)	rs756433029

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