"Genome Diagnostics Laboratory, University Medical Center Utrecht"[sub - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 158525	NM_001005361.3(DNM2):c.235+6A>G	DNM2	Single nucleotide variant (intron variant)	Charcot-Marie-Tooth disease dominant intermediate B +3 more	GBenign/Likely benign
Select item 158524	NM_001005361.3(DNM2):c.235+12C>A	DNM2	Single nucleotide variant (intron variant)	Centronuclear myopathy +4 more	GConflicting classifications of pathogenicity
Select item 382721	NM_001005361.3(DNM2):c.1218C>T (p.Asp406=)	DNM2	Single nucleotide variant (synonymous variant +1 more)	not provided +1 more	GBenign/Likely benign
Select item 7281	NM_001005361.3(DNM2):c.1393C>T (p.Arg465Trp)	DNM2 (R465W)	Single nucleotide variant (missense variant)	Centronuclear myopathy	GPathogenicFDA Recognized database
Select item 158521	NM_001005361.3(DNM2):c.1902C>T (p.Asn634=)	DNM2	Single nucleotide variant (synonymous variant)	Inborn genetic diseases +4 more	GBenign/Likely benign
Select item 158527	NM_001005361.3(DNM2):c.2543+7C>G	DNM2	Single nucleotide variant (intron variant)	Charcot-Marie-Tooth disease dominant intermediate B +4 more	GBenign/Likely benign

ClinVar