List of variants reported as uncertain significance for microcephaly and chorioretinopathy 1 by Fulgent Genetics, Fulgent Genetics

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Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_020461.4(TUBGCP6):c.3288T>G (p.Asp1096Glu)	rs6010209	0.00045
NM_020461.4(TUBGCP6):c.3043G>A (p.Glu1015Lys)	rs149701689	0.00034
NM_020461.4(TUBGCP6):c.2066-6A>G	rs368765755	0.00003
NM_020461.4(TUBGCP6):c.1225C>T (p.Arg409Cys)	rs1282749907	0.00001
NM_020461.4(TUBGCP6):c.2765T>C (p.Leu922Pro)	rs750475050	0.00001

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