rs7169431
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in complete genomics |
Make rs7169431(A;A) |
Make rs7169431(A;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 15 |
Position | 56048698 |
is a | snp |
is | mentioned by |
dbSNP | rs7169431 |
dbSNP (classic) | rs7169431 |
ClinGen | rs7169431 |
ebi | rs7169431 |
HLI | rs7169431 |
Exac | rs7169431 |
Gnomad | rs7169431 |
Varsome | rs7169431 |
LitVar | rs7169431 |
Map | rs7169431 |
PheGenI | rs7169431 |
Biobank | rs7169431 |
1000 genomes | rs7169431 |
hgdp | rs7169431 |
ensembl | rs7169431 |
geneview | rs7169431 |
scholar | rs7169431 |
rs7169431 | |
pharmgkb | rs7169431 |
gwascentral | rs7169431 |
openSNP | rs7169431 |
23andMe | rs7169431 |
SNPshot | rs7169431 |
SNPdbe | rs7169431 |
MSV3d | rs7169431 |
GWAS Ctlg | rs7169431 |
GMAF | 0.1221 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 20062064] |
Trait | Chronic lymphocytic leukemia |
Title | Common variants at 2q37.3, 8q24.21, 15q21.3 abd 16q24.1 influence chronic lymphocytic leukemia risk |
Risk Allele | A |
P-val | 5E-7 |
Odds Ratio | 1.36 [1.21-1.53] |
[PMID 20855867] Inherited genetic susceptibility to monoclonal B-cell lymphocytosis