ClinVar (all) for Orgtrack (Select 280848) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 590886	Single allele		Duplication	Ectrodactyly	GPathogenic
Select item 590885	Single allele	DPCD, BTRC +5 more	Duplication	Ectrodactyly	GPathogenic
Select item 341016	NM_022081.6(HPS4):c.751A>T (p.Thr251Ser)	HPS4 (T251S +2 more)	Single nucleotide variant (missense variant +1 more)	not provided +4 more	GConflicting classifications of pathogenicity
Select item 11407	NM_014009.4(FOXP3):c.1189C>T (p.Arg397Trp)	FOXP3 (R397W +1 more)	Single nucleotide variant (missense variant)	Hydrops fetalis +1 more	GPathogenic

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