ClinVar (all) for Orgtrack (Select 508241) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1299462	NM_058238.3(WNT7B):c.562G>A (p.Gly188Ser)	WNT7B (G188S)	Single nucleotide variant (missense variant)	Matthew-Wood syndrome	GPathogenic
Select item 1299461	NM_058238.3(WNT7B):c.225C>G (p.Tyr75Ter)	WNT7B (Y75*)	Single nucleotide variant (nonsense)	Matthew-Wood syndrome	GPathogenic