C2751084[trait identifier] AND "Baylor Genetics"[submitter] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1027744	NM_144573.4(NEXN):c.178C>T (p.Gln60Ter)	NEXN (Q60*)	Single nucleotide variant (nonsense +1 more)	Dilated cardiomyopathy 1CC +1 more	GUncertain significance
Select item 451638	NM_144573.4(NEXN):c.370G>A (p.Glu124Lys)	LOC126805765, NEXN (E124K +1 more)	Single nucleotide variant (missense variant)	Hypertrophic cardiomyopathy 20 +3 more	GUncertain significance
Select item 1027745	NM_144573.4(NEXN):c.859C>T (p.Gln287Ter)	NEXN (Q223* +1 more)	Single nucleotide variant (nonsense)	Cardiovascular phenotype +1 more	GUncertain significance
Select item 1032442	NM_144573.4(NEXN):c.991G>T (p.Glu331Ter)	NEXN (E267* +1 more)	Single nucleotide variant (nonsense)	Dilated cardiomyopathy 1CC +2 more	GConflicting classifications of pathogenicity
Select item 1027743	NM_144573.4(NEXN):c.1640T>A (p.Ile547Asn)	NEXN (I483N +1 more)	Single nucleotide variant (missense variant)	Hypertrophic cardiomyopathy 20 +1 more	GUncertain significance
Select item 664341	NM_144573.4(NEXN):c.1739G>A (p.Gly580Glu)	NEXN (G580E +1 more)	Single nucleotide variant (missense variant)	Dilated cardiomyopathy 1CC +2 more	GUncertain significance
Select item 326	NM_144573.4(NEXN):c.1955A>G (p.Tyr652Cys)	NEXN (Y652C +1 more)	Single nucleotide variant (missense variant)	Primary dilated cardiomyopathy +5 more	GConflicting classifications of pathogenicity

ClinVar