rs387906684

Orientation

plus

Stabilized

plus

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

Make rs387906684(A;A)

Make rs387906684(A;G)

Reference

GRCh38 38.1/141

Chromosome

2

Position

165367327

Gene

SCN2A

is a	snp
is	mentioned by
dbSNP	rs387906684
dbSNP (classic)	rs387906684
ClinGen	rs387906684
ebi	rs387906684
HLI	rs387906684
Exac	rs387906684
Gnomad	rs387906684
Varsome	rs387906684
LitVar	rs387906684
Map	rs387906684
PheGenI	rs387906684
Biobank	rs387906684
1000 genomes	rs387906684
hgdp	rs387906684
ensembl	rs387906684
geneview	rs387906684
scholar	rs387906684
google	rs387906684
pharmgkb	rs387906684
gwascentral	rs387906684
openSNP	rs387906684
23andMe	rs387906684
SNPshot	rs387906684
SNPdbe	rs387906684
MSV3d	rs387906684
GWAS Ctlg	rs387906684

Max Magnitude

0

ClinVar
Risk	rs387906684(A;A)
Alt	rs387906684(A;A)
Reference	Rs387906684(G;G)
Significance	Other
Disease	Early infantile epileptic encephalopathy 11 Benign familial neonatal-infantile seizures not provided
Variation	info
Gene	SCN2A
CLNDBN	Early infantile epileptic encephalopathy 11 Benign familial neonatal-infantile seizures not provided
Reversed	0
HGVS	NC_000002.11:g.166223837G>A
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000022767.23, RCV000118248.1, RCV000189138.2,