rs1057523786

Orientation

plus

Stabilized

plus

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

Make rs1057523786(A;G)

Make rs1057523786(G;G)

Reference

GRCh38.p7 38.3/150

Chromosome

2

Position

165354262

Gene

SCN2A

is a	snp
is	mentioned by
dbSNP	rs1057523786
dbSNP (classic)	rs1057523786
ClinGen	rs1057523786
ebi	rs1057523786
HLI	rs1057523786
Exac	rs1057523786
Gnomad	rs1057523786
Varsome	rs1057523786
LitVar	rs1057523786
Map	rs1057523786
PheGenI	rs1057523786
Biobank	rs1057523786
1000 genomes	rs1057523786
hgdp	rs1057523786
ensembl	rs1057523786
geneview	rs1057523786
scholar	rs1057523786
google	rs1057523786
pharmgkb	rs1057523786
gwascentral	rs1057523786
openSNP	rs1057523786
23andMe	rs1057523786
SNPshot	rs1057523786
SNPdbe	rs1057523786
MSV3d	rs1057523786
GWAS Ctlg	rs1057523786

Max Magnitude

0

ClinVar
Risk	rs1057523786(G;G)
Alt	rs1057523786(G;G)
Reference	Rs1057523786(A;A)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	SCN2A
CLNDBN	not provided
Reversed	0
HGVS	NC_000002.11:g.166210772A>G
CLNSRC
CLNACC	RCV000438096.1,