ClinVar Miner

List of variants reported as uncertain significance for Microcephaly 2, primary, autosomal recessive, with or without cortical malformations by Institut de Recherche Interdisciplinaire en Biologie Humaine et Moleculaire, Universite Libre de Bruxelles

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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_001083961.2(WDR62):c.253G>A (p.Val85Met)	rs146274964	0.00161
NM_001083961.2(WDR62):c.1640C>T (p.Thr547Met)	rs756313871	0.00005

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