rs1057518373

Orientation

plus

Stabilized

plus

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

Make rs1057518373(C;C)

Make rs1057518373(C;T)

Reference

GRCh38.p7 38.3/150

Chromosome

2

Position

165344766

Gene

SCN2A

is a	snp
is	mentioned by
dbSNP	rs1057518373
dbSNP (classic)	rs1057518373
ClinGen	rs1057518373
ebi	rs1057518373
HLI	rs1057518373
Exac	rs1057518373
Gnomad	rs1057518373
Varsome	rs1057518373
LitVar	rs1057518373
Map	rs1057518373
PheGenI	rs1057518373
Biobank	rs1057518373
1000 genomes	rs1057518373
hgdp	rs1057518373
ensembl	rs1057518373
geneview	rs1057518373
scholar	rs1057518373
google	rs1057518373
pharmgkb	rs1057518373
gwascentral	rs1057518373
openSNP	rs1057518373
23andMe	rs1057518373
SNPshot	rs1057518373
SNPdbe	rs1057518373
MSV3d	rs1057518373
GWAS Ctlg	rs1057518373

Max Magnitude

0

ClinVar
Risk	rs1057518373(C;C)
Alt	rs1057518373(C;C)
Reference	Rs1057518373(T;T)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	SCN2A
CLNDBN	not provided
Reversed	0
HGVS	NC_000002.11:g.166201276T>C
CLNSRC
CLNACC	RCV000413714.1,