rs6851442
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs6851442(A;A) |
Make rs6851442(A;G) |
Make rs6851442(G;G) |
Reference | GRCh38 38.1/142 |
Chromosome | 4 |
Position | 108038126 |
is a | snp |
is | mentioned by |
dbSNP | rs6851442 |
dbSNP (classic) | rs6851442 |
ClinGen | rs6851442 |
ebi | rs6851442 |
HLI | rs6851442 |
Exac | rs6851442 |
Gnomad | rs6851442 |
Varsome | rs6851442 |
LitVar | rs6851442 |
Map | rs6851442 |
PheGenI | rs6851442 |
Biobank | rs6851442 |
1000 genomes | rs6851442 |
hgdp | rs6851442 |
ensembl | rs6851442 |
geneview | rs6851442 |
scholar | rs6851442 |
rs6851442 | |
pharmgkb | rs6851442 |
gwascentral | rs6851442 |
openSNP | rs6851442 |
23andMe | rs6851442 |
SNPshot | rs6851442 |
SNPdbe | rs6851442 |
MSV3d | rs6851442 |
GWAS Ctlg | rs6851442 |
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 |