rs11921451
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs11921451(G;G) |
Make rs11921451(G;T) |
Make rs11921451(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 3 |
Position | 127068316 |
is a | snp |
is | mentioned by |
dbSNP | rs11921451 |
dbSNP (classic) | rs11921451 |
ClinGen | rs11921451 |
ebi | rs11921451 |
HLI | rs11921451 |
Exac | rs11921451 |
Gnomad | rs11921451 |
Varsome | rs11921451 |
LitVar | rs11921451 |
Map | rs11921451 |
PheGenI | rs11921451 |
Biobank | rs11921451 |
1000 genomes | rs11921451 |
hgdp | rs11921451 |
ensembl | rs11921451 |
geneview | rs11921451 |
scholar | rs11921451 |
rs11921451 | |
pharmgkb | rs11921451 |
gwascentral | rs11921451 |
openSNP | rs11921451 |
23andMe | rs11921451 |
SNPshot | rs11921451 |
SNPdbe | rs11921451 |
MSV3d | rs11921451 |
GWAS Ctlg | rs11921451 |
Max Magnitude | 0 |
? | (G;G) (G;T) (T;T) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 24529757] |
Trait | Amyotrophic lateral sclerosis (sporadic) |
Title | A genome-wide association study combining pathway analysis for typical sporadic amyotrophic lateral sclerosis in Chinese Han populations. |
Risk Allele | |
P-val | 5E-6 |
Odds Ratio | NR NR |