List of variants in gene RAPGEF2 reported as uncertain significance for electroclinical syndrome

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_001394067.2(RAPGEF2):c.4958-8A>G	rs1732314095
NM_001394067.2(RAPGEF2):c.4975G>A (p.Ala1659Thr)
NM_001394067.2(RAPGEF2):c.819G>C (p.Glu273Asp)	rs1764342195

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