rs11062578
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs11062578(A;A) |
Make rs11062578(A;G) |
Make rs11062578(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 12 |
Position | 3218001 |
Gene | TSPAN9 |
is a | snp |
is | mentioned by |
dbSNP | rs11062578 |
dbSNP (classic) | rs11062578 |
ClinGen | rs11062578 |
ebi | rs11062578 |
HLI | rs11062578 |
Exac | rs11062578 |
Gnomad | rs11062578 |
Varsome | rs11062578 |
LitVar | rs11062578 |
Map | rs11062578 |
PheGenI | rs11062578 |
Biobank | rs11062578 |
1000 genomes | rs11062578 |
hgdp | rs11062578 |
ensembl | rs11062578 |
geneview | rs11062578 |
scholar | rs11062578 |
rs11062578 | |
pharmgkb | rs11062578 |
gwascentral | rs11062578 |
openSNP | rs11062578 |
23andMe | rs11062578 |
SNPshot | rs11062578 |
SNPdbe | rs11062578 |
MSV3d | rs11062578 |
GWAS Ctlg | rs11062578 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 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 | 3E-6 |
Odds Ratio | NR NR |