ClinVar Miner

Submissions for variant NM_001165963.4(SCN1A):c.5225A>G (p.Asp1742Gly)

dbSNP: rs121918812

Minimum review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
		ClinVar version:

Total submissions: 1

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Submitter	RCV	SCV	Clinical significance	Condition	Last evaluated	Review status	Method	Comment
UniProtKB/Swiss-Prot	RCV000059533	SCV000091065	not provided	Generalized epilepsy with febrile seizures plus, type 1		no assertion provided	not provided

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