rs1057517853

Orientation

plus

Stabilized

plus

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

Make rs1057517853(C;C)

Make rs1057517853(C;T)

Reference

GRCh38.p7 38.3/150

Chromosome

2

Position

165388667

Gene

SCN2A

is a	snp
is	mentioned by
dbSNP	rs1057517853
dbSNP (classic)	rs1057517853
ClinGen	rs1057517853
ebi	rs1057517853
HLI	rs1057517853
Exac	rs1057517853
Gnomad	rs1057517853
Varsome	rs1057517853
LitVar	rs1057517853
Map	rs1057517853
PheGenI	rs1057517853
Biobank	rs1057517853
1000 genomes	rs1057517853
hgdp	rs1057517853
ensembl	rs1057517853
geneview	rs1057517853
scholar	rs1057517853
google	rs1057517853
pharmgkb	rs1057517853
gwascentral	rs1057517853
openSNP	rs1057517853
23andMe	rs1057517853
SNPshot	rs1057517853
SNPdbe	rs1057517853
MSV3d	rs1057517853
GWAS Ctlg	rs1057517853

Max Magnitude

0

ClinVar
Risk	rs1057517853(C;C)
Alt	rs1057517853(C;C)
Reference	Rs1057517853(T;T)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	SCN2A
CLNDBN	not provided
Reversed	0
HGVS	NC_000002.11:g.166245177T>C
CLNSRC
CLNACC	RCV000414308.1,