C4015285[trait identifier] AND "New York Genome Center"[submitter] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2584599	NM_001382280.1(LRRC53):c.2630C>T (p.Ala877Val)	FPGT-TNNI3K, LRRC53 +1 more (A845V +1 more)	Single nucleotide variant (missense variant +1 more)	Atrial conduction disease	GUncertain significance
Select item 1679708	NM_001382280.1(LRRC53):c.2543_2546dup (p.Glu849delinsAspTer)	FPGT-TNNI3K, LRRC53 +1 more	Duplication (nonsense +1 more)	Atrial conduction disease	GUncertain significance