rs387906687

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(A;A)	0	common in clinvar

Make rs387906687(A;G)

Make rs387906687(G;G)

Reference

GRCh38 38.1/141

Chromosome

2

Position

165310379

Gene

SCN2A

is a	snp
is	mentioned by
dbSNP	rs387906687
dbSNP (classic)	rs387906687
ClinGen	rs387906687
ebi	rs387906687
HLI	rs387906687
Exac	rs387906687
Gnomad	rs387906687
Varsome	rs387906687
LitVar	rs387906687
Map	rs387906687
PheGenI	rs387906687
Biobank	rs387906687
1000 genomes	rs387906687
hgdp	rs387906687
ensembl	rs387906687
geneview	rs387906687
scholar	rs387906687
google	rs387906687
pharmgkb	rs387906687
gwascentral	rs387906687
openSNP	rs387906687
23andMe	rs387906687
SNPshot	rs387906687
SNPdbe	rs387906687
MSV3d	rs387906687
GWAS Ctlg	rs387906687

Max Magnitude

0

ClinVar
Risk	rs387906687(G;G)
Alt	rs387906687(G;G)
Reference	Rs387906687(A;A)
Significance	Pathogenic
Disease	Benign familial neonatal-infantile seizures
Variation	info
Gene	SCN2A
CLNDBN	Benign familial neonatal-infantile seizures
Reversed	0
HGVS	NC_000002.11:g.166166889A>G
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000022770.18,