List of variants reported as uncertain significance for Microcephaly 20, primary, autosomal recessive 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_014875.3(KIF14):c.1813G>T (p.Ala605Ser)	rs370591311	0.00007
NM_014875.3(KIF14):c.1979+2C>T	rs1558083294
NM_014875.3(KIF14):c.378_383dup (p.Thr127_Asp128insGluThr)	rs2527807220
NM_014875.3(KIF14):c.4353+7T>A	rs1410610212

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