rs4363506
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs4363506(C;C) |
Make rs4363506(C;T) |
Make rs4363506(T;T) |
Reference | GRCh38 38.1/142 |
Chromosome | 10 |
Position | 127476239 |
is a | snp |
is | mentioned by |
dbSNP | rs4363506 |
dbSNP (classic) | rs4363506 |
ClinGen | rs4363506 |
ebi | rs4363506 |
HLI | rs4363506 |
Exac | rs4363506 |
Gnomad | rs4363506 |
Varsome | rs4363506 |
LitVar | rs4363506 |
Map | rs4363506 |
PheGenI | rs4363506 |
Biobank | rs4363506 |
1000 genomes | rs4363506 |
hgdp | rs4363506 |
ensembl | rs4363506 |
geneview | rs4363506 |
scholar | rs4363506 |
rs4363506 | |
pharmgkb | rs4363506 |
gwascentral | rs4363506 |
openSNP | rs4363506 |
23andMe | rs4363506 |
SNPshot | rs4363506 |
SNPdbe | rs4363506 |
MSV3d | rs4363506 |
GWAS Ctlg | rs4363506 |
GMAF | 0.4789 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
GWAS | |
---|---|
SNP | rs4363506 |
PubMedID | [PMID 17362836] |
Condition | Amyotrophic lateral sclerosis |
Gene | Intergenic |
Risk Allele | |
pValue | 7.00E-007 |
OR | 1.9 |
95% CI | 1.50-2.40 |
[PMID 19740415] Genome-wide association reveals three SNPs associated with sporadic amyotrophic lateral sclerosis through a two-locus analysis