rs1057523696

Orientation

plus

Stabilized

plus

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

Make rs1057523696(C;C)

Make rs1057523696(C;T)

Reference

GRCh38.p7 38.3/150

Chromosome

2

Position

165344867

Gene

SCN2A

is a	snp
is	mentioned by
dbSNP	rs1057523696
dbSNP (classic)	rs1057523696
ClinGen	rs1057523696
ebi	rs1057523696
HLI	rs1057523696
Exac	rs1057523696
Gnomad	rs1057523696
Varsome	rs1057523696
LitVar	rs1057523696
Map	rs1057523696
PheGenI	rs1057523696
Biobank	rs1057523696
1000 genomes	rs1057523696
hgdp	rs1057523696
ensembl	rs1057523696
geneview	rs1057523696
scholar	rs1057523696
google	rs1057523696
pharmgkb	rs1057523696
gwascentral	rs1057523696
openSNP	rs1057523696
23andMe	rs1057523696
SNPshot	rs1057523696
SNPdbe	rs1057523696
MSV3d	rs1057523696
GWAS Ctlg	rs1057523696

Max Magnitude

0

ClinVar
Risk	rs1057523696(C;C)
Alt	rs1057523696(C;C)
Reference	Rs1057523696(T;T)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	SCN2A
CLNDBN	not provided
Reversed	0
HGVS	NC_000002.11:g.166201377T>C
CLNSRC
CLNACC	RCV000422689.1,