List of variants reported as uncertain significance for central nervous system malformation by Al Jalila Children’s Genomics Center, Al Jalila Childrens Speciality Hospital

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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_001378615.1(CC2D2A):c.3601G>A (p.Gly1201Arg)	rs1392733763	0.00001
NM_002547.3(OPHN1):c.1139T>C (p.Met380Thr)	rs770608210	0.00001

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