ClinVar Miner

List of variants in gene FGF13 reported as uncertain significance for Developmental and epileptic encephalopathy, 90; Intellectual developmental disorder, X-linked 110

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: 1

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HGVS	dbSNP	gnomAD frequency
NM_001139500.2(FGF13):c.116C>T (p.Ala39Val)

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