rs11618202
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common on affy axiom data |
Make rs11618202(G;G) |
Make rs11618202(G;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 13 |
Position | 30539242 |
Gene | HMGB1 |
is a | snp |
is | mentioned by |
dbSNP | rs11618202 |
dbSNP (classic) | rs11618202 |
ClinGen | rs11618202 |
ebi | rs11618202 |
HLI | rs11618202 |
Exac | rs11618202 |
Gnomad | rs11618202 |
Varsome | rs11618202 |
LitVar | rs11618202 |
Map | rs11618202 |
PheGenI | rs11618202 |
Biobank | rs11618202 |
1000 genomes | rs11618202 |
hgdp | rs11618202 |
ensembl | rs11618202 |
geneview | rs11618202 |
scholar | rs11618202 |
rs11618202 | |
pharmgkb | rs11618202 |
gwascentral | rs11618202 |
openSNP | rs11618202 |
23andMe | rs11618202 |
SNPshot | rs11618202 |
SNPdbe | rs11618202 |
MSV3d | rs11618202 |
GWAS Ctlg | rs11618202 |
GMAF | 0.06336 |
Max Magnitude | 0 |
? | (G;G) (G;T) (T;T) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 21116278] |
Trait | |
Title | Genome-wide association with MRI atrophy measures as a quantitative trait locus for Alzheimer's disease |
Risk Allele | |
P-val | 0.000007 |
Odds Ratio | 0.0003 [NR] unit decrease (main effect) |