ClinVar Miner

List of variants reported as pathogenic for Microcephaly 2, primary, autosomal recessive, with or without cortical malformations by Victorian Clinical Genetics Services, Murdoch Childrens Research Institute

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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_001083961.2(WDR62):c.1043+3A>G	rs587784541	0.00009
NM_001083961.2(WDR62):c.2984C>G (p.Ser995Ter)
NM_001083961.2(WDR62):c.3863G>A (p.Trp1288Ter)

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