"Blueprint Genetics"[submitter] AND "LOC126806422"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 180574	NM_001267550.2(TTN):c.69783G>A (p.Trp23261Ter)	LOC126806422, TTN +1 more (W23261* +5 more)	Single nucleotide variant (nonsense)	Primary dilated cardiomyopathy	GLikely pathogenic
Select item 222877	NM_001267550.2(TTN):c.69639dup (p.Val23214fs)	LOC126806422, TTN +1 more (V20646fs +5 more)	Duplication (frameshift variant)	Primary dilated cardiomyopathy	GLikely pathogenic