ClinVar Miner

List of variants reported as uncertain significance for X-linked complicated corpus callosum dysgenesis

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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_001278116.2(L1CAM):c.3163G>A (p.Gly1055Arg)	rs1484399991	0.00001
NM_001278116.2(L1CAM):c.1430A>C (p.Tyr477Ser)
NM_001278116.2(L1CAM):c.3754C>T (p.Pro1252Ser)	rs2064673421

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