ClinVar Miner

List of variants reported as uncertain significance for Microcephaly 18, primary, autosomal dominant by Victorian Clinical Genetics Services, Murdoch Childrens Research Institute

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_014991.6(WDFY3):c.3473T>G (p.Leu1158Arg)	rs2149575345
NM_014991.6(WDFY3):c.4518+7A>G
NM_014991.6(WDFY3):c.7189G>T (p.Val2397Leu)
NM_014991.6(WDFY3):c.7324A>C (p.Met2442Leu)

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