List of variants in gene EMX2 reported as pathogenic for Schizencephaly

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_004098.4(EMX2):c.407-1G>A	rs1564751655
NM_004098.4(EMX2):c.407-4G>T	rs1411887961
NM_004098.4(EMX2):c.407G>T (p.Gly136Val)	rs755549724
NM_004098.4(EMX2):c.575_576insA (p.Ser192fs)	rs2133969658

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