List of variants in gene combination EMX2, EMX2OS reported as uncertain significance for Inborn genetic diseases

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: 8

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HGVS	dbSNP	gnomAD frequency
NM_004098.4(EMX2):c.311C>T (p.Ser104Leu)	rs532461355	0.00001
NM_004098.4(EMX2):c.101C>T (p.Ala34Val)	rs2493087919
NM_004098.4(EMX2):c.13G>C (p.Ala5Pro)
NM_004098.4(EMX2):c.14C>G (p.Ala5Gly)	rs540731987
NM_004098.4(EMX2):c.157T>A (p.Ser53Thr)
NM_004098.4(EMX2):c.211T>G (p.Phe71Val)
NM_004098.4(EMX2):c.238A>G (p.Asn80Asp)	rs770506828
NM_004098.4(EMX2):c.308A>T (p.His103Leu)

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