ClinVar for MedGen (Select 436211) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 374054	NM_001083962.2(TCF4):c.500-1G>A	TCF4	Single nucleotide variant (splice acceptor variant)	Global developmental delay +7 more	GPathogenic
Select item 268039	46;XY;t(3;18)(q13.31;q22.1)dn		Translocation	Intention tremor +29 more	GPathogenic
Select item 267843	46;XX;t(2;8)(q33.1;q24.3)dn		Translocation	Feeding difficulties in infancy +2 more	GUncertain significance

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