"Laboratory of Diagnostic Genome Analysis, Leiden University Medical C - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 47159	NM_001267550.2(TTN):c.60055G>A (p.Glu20019Lys)	LOC126806424, TTN +1 more (E20019K +5 more)	Single nucleotide variant (missense variant)	Cardiovascular phenotype +8 more	GBenign/Likely benign
Select item 47148	NM_001267550.2(TTN):c.59315C>T (p.Pro19772Leu)	LOC126806424, TTN +1 more (P19772L +5 more)	Single nucleotide variant (missense variant)	Cardiovascular phenotype +7 more	GBenign/Likely benign