rs982274
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs982274(G;G) |
Make rs982274(G;T) |
Make rs982274(T;T) |
Reference | GRCh38 38.1/142 |
Chromosome | 21 |
Position | 18107413 |
Gene | CHODL |
is a | snp |
is | mentioned by |
dbSNP | rs982274 |
dbSNP (classic) | rs982274 |
ClinGen | rs982274 |
ebi | rs982274 |
HLI | rs982274 |
Exac | rs982274 |
Gnomad | rs982274 |
Varsome | rs982274 |
LitVar | rs982274 |
Map | rs982274 |
PheGenI | rs982274 |
Biobank | rs982274 |
1000 genomes | rs982274 |
hgdp | rs982274 |
ensembl | rs982274 |
geneview | rs982274 |
scholar | rs982274 |
rs982274 | |
pharmgkb | rs982274 |
gwascentral | rs982274 |
openSNP | rs982274 |
23andMe | rs982274 |
SNPshot | rs982274 |
SNPdbe | rs982274 |
MSV3d | rs982274 |
GWAS Ctlg | rs982274 |
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 | 6E-6 |
Odds Ratio | NR NR |