List of variants reported as uncertain significance for Microcephaly 1, primary, autosomal recessive by Fulgent Genetics, Fulgent Genetics

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Total variants: 12

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HGVS	dbSNP	gnomAD frequency
NM_024596.5(MCPH1):c.1349A>C (p.Lys450Thr)	rs77959215	0.00160
NM_024596.5(MCPH1):c.2180C>T (p.Pro727Leu)	rs199861426	0.00086
NM_024596.5(MCPH1):c.1273T>A (p.Tyr425Asn)	rs201261159	0.00067
NM_024596.5(MCPH1):c.783T>A (p.Asp261Glu)	rs199700538	0.00046
NM_024596.5(MCPH1):c.775A>C (p.Lys259Gln)	rs375695403	0.00018
NM_024596.5(MCPH1):c.2108G>A (p.Arg703His)	rs370275760	0.00013
NM_024596.5(MCPH1):c.1186C>A (p.His396Asn)	rs201128010	0.00010
NM_024596.5(MCPH1):c.1679G>T (p.Ser560Ile)	rs201405704	0.00010
NM_024596.5(MCPH1):c.2395C>T (p.Pro799Ser)	rs369127299	0.00008
NM_024596.5(MCPH1):c.1477C>T (p.Arg493Cys)	rs757646355	0.00006
NM_024596.5(MCPH1):c.2105C>T (p.Ala702Val)	rs751512309	0.00003
NM_024596.5(MCPH1):c.2257G>A (p.Gly753Arg)	rs587783737

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