Related gene-specific medical variations for Gene (Select 57216) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2690436	NM_020335.3(VANGL2):c.233C>T (p.Thr78Ile)	VANGL2 (T78I)	Single nucleotide variant (missense variant)	Neural tube defect	GUncertain significance
Select item 2672275	NM_020335.3(VANGL2):c.403C>T (p.Arg135Trp)	VANGL2 (R135W)	Single nucleotide variant (missense variant)	Neural tube defect	GBenign
Select item 2438509	NM_020335.3(VANGL2):c.986C>T (p.Ala329Val)	VANGL2 (A329V)	Single nucleotide variant (missense variant)	Neural tube defect	GUncertain significance

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