rs386965
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs386965(A;A) |
Make rs386965(A;G) |
Make rs386965(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 16 |
Position | 79618644 |
is a | snp |
is | mentioned by |
dbSNP | rs386965 |
dbSNP (classic) | rs386965 |
ClinGen | rs386965 |
ebi | rs386965 |
HLI | rs386965 |
Exac | rs386965 |
Gnomad | rs386965 |
Varsome | rs386965 |
LitVar | rs386965 |
Map | rs386965 |
PheGenI | rs386965 |
Biobank | rs386965 |
1000 genomes | rs386965 |
hgdp | rs386965 |
ensembl | rs386965 |
geneview | rs386965 |
scholar | rs386965 |
rs386965 | |
pharmgkb | rs386965 |
gwascentral | rs386965 |
openSNP | rs386965 |
23andMe | rs386965 |
SNPshot | rs386965 |
SNPdbe | rs386965 |
MSV3d | rs386965 |
GWAS Ctlg | rs386965 |
GMAF | 0.3737 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 21833088![]() |
Trait | Multiple sclerosis |
Title | Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis. |
Risk Allele | G |
P-val | 4E-6 |
Odds Ratio | 1.09 [1.07-1.11] |