rs1057521747

Orientation

plus

Stabilized

plus

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

Make rs1057521747(C;C)

Make rs1057521747(C;G)

Reference

GRCh38.p7 38.3/150

Chromosome

2

Position

165386976

Gene

SCN2A

is a	snp
is	mentioned by
dbSNP	rs1057521747
dbSNP (classic)	rs1057521747
ClinGen	rs1057521747
ebi	rs1057521747
HLI	rs1057521747
Exac	rs1057521747
Gnomad	rs1057521747
Varsome	rs1057521747
LitVar	rs1057521747
Map	rs1057521747
PheGenI	rs1057521747
Biobank	rs1057521747
1000 genomes	rs1057521747
hgdp	rs1057521747
ensembl	rs1057521747
geneview	rs1057521747
scholar	rs1057521747
google	rs1057521747
pharmgkb	rs1057521747
gwascentral	rs1057521747
openSNP	rs1057521747
23andMe	rs1057521747
SNPshot	rs1057521747
SNPdbe	rs1057521747
MSV3d	rs1057521747
GWAS Ctlg	rs1057521747

Max Magnitude

0

ClinVar
Risk	rs1057521747(C;C)
Alt	rs1057521747(C;C)
Reference	Rs1057521747(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	SCN2A
CLNDBN	not provided
Reversed	0
HGVS	NC_000002.11:g.166243486G>C
CLNSRC
CLNACC	RCV000432281.1,