ClinVar (all) for Orgtrack (Select 507771) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 984916	NR_134676.1(LOC105374344):n.52T>C	LOC105374344, RNF212	Single nucleotide variant (non-coding transcript variant)	Down syndrome	Grisk factor
Select item 981242	NC_000023.11:g.946718C>G		Single nucleotide variant	Sudden infant death-dysgenesis of the testes syndrome	GLikely pathogenic