rs1057519525

Orientation

plus

Stabilized

plus

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

Make rs1057519525(G;G)

Make rs1057519525(G;T)

Reference

GRCh38.p7 38.3/150

Chromosome

2

Position

165308760

Gene

SCN2A

is a	snp
is	mentioned by
dbSNP	rs1057519525
dbSNP (classic)	rs1057519525
ClinGen	rs1057519525
ebi	rs1057519525
HLI	rs1057519525
Exac	rs1057519525
Gnomad	rs1057519525
Varsome	rs1057519525
LitVar	rs1057519525
Map	rs1057519525
PheGenI	rs1057519525
Biobank	rs1057519525
1000 genomes	rs1057519525
hgdp	rs1057519525
ensembl	rs1057519525
geneview	rs1057519525
scholar	rs1057519525
google	rs1057519525
pharmgkb	rs1057519525
gwascentral	rs1057519525
openSNP	rs1057519525
23andMe	rs1057519525
SNPshot	rs1057519525
SNPdbe	rs1057519525
MSV3d	rs1057519525
GWAS Ctlg	rs1057519525

Max Magnitude

0

ClinVar
Risk	rs1057519525(G;G)
Alt	rs1057519525(G;G)
Reference	Rs1057519525(T;T)
Significance	Probable-Pathogenic
Disease	Focal epilepsy
Variation	info
Gene	SCN2A
CLNDBN	Focal epilepsy
Reversed	0
HGVS	NC_000002.11:g.166165270T>G
CLNSRC
CLNACC	RCV000416990.1,