List of variants reported as likely pathogenic for anencephaly

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_031307.4(PUS3):c.838C>T (p.Arg280Ter)	rs374443634	0.00002
NM_031307.4(PUS3):c.340T>C (p.Cys114Arg)	rs752052349	0.00001
NM_001163809.2(WDR81):c.845G>A (p.Gly282Glu)	rs730882206
NM_001378615.1(CC2D2A):c.1497del (p.Glu500fs)	rs2109029810

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