ClinVar for MedGen (Select 66809) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 523380	NM_000553.6(WRN):c.724+1G>T	WRN	Single nucleotide variant (splice donor variant)	Werner syndrome +6 more	GPathogenic/Likely pathogenic
Select item 268009	46;X;t(X;3)(p21.3;p25.1)dn		Translocation	Dolichocephaly +11 more	GPathogenic