rs4406737
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs4406737(A;A) |
Make rs4406737(A;G) |
Make rs4406737(G;G) |
Reference | GRCh38 38.1/142 |
Chromosome | 10 |
Position | 88999967 |
Gene | FAS |
is a | snp |
is | mentioned by |
dbSNP | rs4406737 |
dbSNP (classic) | rs4406737 |
ClinGen | rs4406737 |
ebi | rs4406737 |
HLI | rs4406737 |
Exac | rs4406737 |
Gnomad | rs4406737 |
Varsome | rs4406737 |
LitVar | rs4406737 |
Map | rs4406737 |
PheGenI | rs4406737 |
Biobank | rs4406737 |
1000 genomes | rs4406737 |
hgdp | rs4406737 |
ensembl | rs4406737 |
geneview | rs4406737 |
scholar | rs4406737 |
rs4406737 | |
pharmgkb | rs4406737 |
gwascentral | rs4406737 |
openSNP | rs4406737 |
23andMe | rs4406737 |
SNPshot | rs4406737 |
SNPdbe | rs4406737 |
MSV3d | rs4406737 |
GWAS Ctlg | rs4406737 |
GMAF | 0.4922 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 23770605![]() |
Trait | Chronic lymphocytic leukemia |
Title | Genome-wide association study identifies multiple risk loci for chronic lymphocytic leukemia. |
Risk Allele | G |
P-val | 1E-14 |
Odds Ratio | 1.27 [1.19-1.33] |