rs305061
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs305061(C;C) |
Make rs305061(C;T) |
Make rs305061(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 16 |
Position | 85942053 |
is a | snp |
is | mentioned by |
dbSNP | rs305061 |
dbSNP (classic) | rs305061 |
ClinGen | rs305061 |
ebi | rs305061 |
HLI | rs305061 |
Exac | rs305061 |
Gnomad | rs305061 |
Varsome | rs305061 |
LitVar | rs305061 |
Map | rs305061 |
PheGenI | rs305061 |
Biobank | rs305061 |
1000 genomes | rs305061 |
hgdp | rs305061 |
ensembl | rs305061 |
geneview | rs305061 |
scholar | rs305061 |
rs305061 | |
pharmgkb | rs305061 |
gwascentral | rs305061 |
openSNP | rs305061 |
23andMe | rs305061 |
SNPshot | rs305061 |
SNPdbe | rs305061 |
MSV3d | rs305061 |
GWAS Ctlg | rs305061 |
GMAF | 0.2346 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 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 | T |
P-val | 4E-7 |
Odds Ratio | 1.22 [1.12-1.32] |
[PMID 20855867] Inherited genetic susceptibility to monoclonal B-cell lymphocytosis
GWAS snp | |
---|---|
PMID | [PMID 22700719] |
Trait | |
Title | Common variation at 6p21.31 (BAK1) influences the risk of chronic lymphocytic leukemia. |
Risk Allele | |
P-val | 9E-8 |
Odds Ratio | 1.3300 None |