rs4761659
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs4761659(C;C) |
Make rs4761659(C;T) |
Make rs4761659(T;T) |
Reference | GRCh38 38.1/142 |
Chromosome | 12 |
Position | 93293308 |
Gene | LOC643339 |
is a | snp |
is | mentioned by |
dbSNP | rs4761659 |
dbSNP (classic) | rs4761659 |
ClinGen | rs4761659 |
ebi | rs4761659 |
HLI | rs4761659 |
Exac | rs4761659 |
Gnomad | rs4761659 |
Varsome | rs4761659 |
LitVar | rs4761659 |
Map | rs4761659 |
PheGenI | rs4761659 |
Biobank | rs4761659 |
1000 genomes | rs4761659 |
hgdp | rs4761659 |
ensembl | rs4761659 |
geneview | rs4761659 |
scholar | rs4761659 |
rs4761659 | |
pharmgkb | rs4761659 |
gwascentral | rs4761659 |
openSNP | rs4761659 |
23andMe | rs4761659 |
SNPshot | rs4761659 |
SNPdbe | rs4761659 |
MSV3d | rs4761659 |
GWAS Ctlg | rs4761659 |
Max Magnitude | 0 |
? | (C;C) (C;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 | 3E-7 |
Odds Ratio | NR NR |