C3151039[trait identifier] AND "Genome Diagnostics Laboratory, Univers - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 522273	NM_001032283.3(TMPO):c.280-8G>A	TMPO	Single nucleotide variant (intron variant)	Dilated cardiomyopathy 1T +1 more	GBenign/Likely benign
Select item 44662	NM_001032283.3(TMPO):c.565+1665A>G	TMPO (K416E)	Single nucleotide variant (missense variant +1 more)	not specified +3 more	GBenign
Select item 192133	NM_001032283.3(TMPO):c.565+1696C>T	TMPO (P426L)	Single nucleotide variant (missense variant +1 more)	Primary dilated cardiomyopathy +6 more	GConflicting classifications of pathogenicity

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