List of variants in gene SCN1A reported as uncertain significance by Lifecell International Pvt. Ltd

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: 7

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HGVS	dbSNP	gnomAD frequency
NM_001165963.4(SCN1A):c.136G>A (p.Glu46Lys)	rs769582667	0.00003
NM_001165963.4(SCN1A):c.1982C>T (p.Thr661Ile)	rs780340848	0.00001
NM_001165963.4(SCN1A):c.2006C>T (p.Pro669Leu)	rs570326929	0.00001
NM_001165963.4(SCN1A):c.2552A>G (p.Asn851Ser)	rs561912072	0.00001
NM_001165963.4(SCN1A):c.1423_1424delinsCT (p.Ala475Leu)	rs2105852411
NM_001165963.4(SCN1A):c.1719C>G (p.Ser573Arg)	rs748767737
NM_001165963.4(SCN1A):c.2164A>C (p.Asn722His)	rs1341631584

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