rs602594
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs602594(A;A) |
Make rs602594(A;G) |
Make rs602594(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 11 |
Position | 118169895 |
Gene | SCN2B |
is a | snp |
is | mentioned by |
dbSNP | rs602594 |
dbSNP (classic) | rs602594 |
ClinGen | rs602594 |
ebi | rs602594 |
HLI | rs602594 |
Exac | rs602594 |
Gnomad | rs602594 |
Varsome | rs602594 |
LitVar | rs602594 |
Map | rs602594 |
PheGenI | rs602594 |
Biobank | rs602594 |
1000 genomes | rs602594 |
hgdp | rs602594 |
ensembl | rs602594 |
geneview | rs602594 |
scholar | rs602594 |
rs602594 | |
pharmgkb | rs602594 |
gwascentral | rs602594 |
openSNP | rs602594 |
23andMe | rs602594 |
SNPshot | rs602594 |
SNPdbe | rs602594 |
MSV3d | rs602594 |
GWAS Ctlg | rs602594 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 24337656] Case-control association study of polymorphisms in the voltage-gated sodium channel genes SCN1A, SCN2A, SCN3A, SCN1B, and SCN2B and epilepsy