rs3809263
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs3809263(A;A) |
Make rs3809263(A;G) |
Make rs3809263(G;G) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 12 |
Position | 664290 |
Gene | NINJ2 |
is a | snp |
is | mentioned by |
dbSNP | rs3809263 |
dbSNP (classic) | rs3809263 |
ClinGen | rs3809263 |
ebi | rs3809263 |
HLI | rs3809263 |
Exac | rs3809263 |
Gnomad | rs3809263 |
Varsome | rs3809263 |
LitVar | rs3809263 |
Map | rs3809263 |
PheGenI | rs3809263 |
Biobank | rs3809263 |
1000 genomes | rs3809263 |
hgdp | rs3809263 |
ensembl | rs3809263 |
geneview | rs3809263 |
scholar | rs3809263 |
rs3809263 | |
pharmgkb | rs3809263 |
gwascentral | rs3809263 |
openSNP | rs3809263 |
23andMe | rs3809263 |
SNPshot | rs3809263 |
SNPdbe | rs3809263 |
MSV3d | rs3809263 |
GWAS Ctlg | rs3809263 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 26687183] A Novel Functional Polymorphism in the NINJ2 Promoter Predicts Risk of Large Artery Atherosclerotic Stroke.
[PMID 31292852] A single nucleotide polymorphism within Ninjurin 2 is associated with risk of multiple sclerosis.