ClinVar (all) for Orgtrack (Select 505325) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 162222	NM_001987.5(ETV6):c.641C>T (p.Pro214Leu)	ETV6	Single nucleotide variant (missense variant)	Thrombocytopenia 5 +1 more	GPathogenic/Likely pathogenic
Select item 162221	NM_001987.5(ETV6):c.1106G>A (p.Arg369Gln)	ETV6, LOC126861452	Single nucleotide variant (missense variant)	Thrombocytopenia 5 +3 more	GPathogenic/Likely pathogenic
Select item 162220	NM_001987.5(ETV6):c.1195C>T (p.Arg399Cys)	ETV6	Single nucleotide variant (missense variant)	not provided +1 more	GPathogenic

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