List of variants in gene L1CAM reported as likely benign for MASA syndrome; X-linked complicated corpus callosum dysgenesis; X-linked hydrocephalus syndrome

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_001278116.2(L1CAM):c.2657G>A (p.Arg886Gln)	rs142603269	0.00028
NM_001278116.2(L1CAM):c.113C>T (p.Thr38Met)	rs201151358	0.00027
NM_001278116.2(L1CAM):c.3760G>A (p.Val1254Met)	rs200498314	0.00006

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