List of variants reported as likely benign for microcephaly 6, primary, autosomal recessive by Illumina Laboratory Services, Illumina

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_018451.5(CPAP):c.1233G>A (p.Pro411=)	rs112133852	0.00368
NM_018451.5(CPAP):c.*570T>C	rs139596189	0.00313
NM_018451.5(CPAP):c.2806A>G (p.Ser936Gly)	rs75008861	0.00070
NM_018451.5(CPAP):c.763A>G (p.Thr255Ala)	rs150932292	0.00053

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