ClinVar Miner

List of variants in gene combination LOC102724058, SCN1A reported by Clinical Molecular Genetics Laboratory, Johns Hopkins All Children's Hospital

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_001165963.4(SCN1A):c.3623G>A (p.Arg1208Lys)	rs1559149025
NM_001165963.4(SCN1A):c.3851G>A (p.Trp1284Ter)	rs1559144583

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