rs1488902
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs1488902(C;C) |
Make rs1488902(C;T) |
Make rs1488902(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 11 |
Position | 89611857 |
is a | snp |
is | mentioned by |
dbSNP | rs1488902 |
dbSNP (classic) | rs1488902 |
ClinGen | rs1488902 |
ebi | rs1488902 |
HLI | rs1488902 |
Exac | rs1488902 |
Gnomad | rs1488902 |
Varsome | rs1488902 |
LitVar | rs1488902 |
Map | rs1488902 |
PheGenI | rs1488902 |
Biobank | rs1488902 |
1000 genomes | rs1488902 |
hgdp | rs1488902 |
ensembl | rs1488902 |
geneview | rs1488902 |
scholar | rs1488902 |
rs1488902 | |
pharmgkb | rs1488902 |
gwascentral | rs1488902 |
openSNP | rs1488902 |
23andMe | rs1488902 |
SNPshot | rs1488902 |
SNPdbe | rs1488902 |
MSV3d | rs1488902 |
GWAS Ctlg | rs1488902 |
GMAF | 0.3999 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 20801717] |
Trait | |
Title | Chromosome 9p21 in sporadic amyotrophic lateral sclerosis in the UK and seven other countries: a genome-wide association study |
Risk Allele | C |
P-val | 0.000003 |
Odds Ratio | 1.1450 [NR] |