rs210142
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs210142(C;C) |
Make rs210142(C;T) |
Make rs210142(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 33579060 |
Gene | BAK1 |
is a | snp |
is | mentioned by |
dbSNP | rs210142 |
dbSNP (classic) | rs210142 |
ClinGen | rs210142 |
ebi | rs210142 |
HLI | rs210142 |
Exac | rs210142 |
Gnomad | rs210142 |
Varsome | rs210142 |
LitVar | rs210142 |
Map | rs210142 |
PheGenI | rs210142 |
Biobank | rs210142 |
1000 genomes | rs210142 |
hgdp | rs210142 |
ensembl | rs210142 |
geneview | rs210142 |
scholar | rs210142 |
rs210142 | |
pharmgkb | rs210142 |
gwascentral | rs210142 |
openSNP | rs210142 |
23andMe | rs210142 |
SNPshot | rs210142 |
SNPdbe | rs210142 |
MSV3d | rs210142 |
GWAS Ctlg | rs210142 |
GMAF | 0.2493 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 22700719] |
Trait | |
Title | Common variation at 6p21.31 (BAK1) influences the risk of chronic lymphocytic leukemia. |
Risk Allele | C |
P-val | 9E-16 |
Odds Ratio | 1.4000 None |
GWAS snp | |
---|---|
PMID | [PMID 23770605] |
Trait | Chronic lymphocytic leukemia |
Title | Genome-wide association study identifies multiple risk loci for chronic lymphocytic leukemia. |
Risk Allele | C |
P-val | 5E-8 |
Odds Ratio | 1.22 [NR] |
[PMID 23025533] Common variants within 6p21.31 locus are associated with chronic lymphocytic leukaemia and, potentially, other non-Hodgkin lymphoma subtypes.
[PMID 32467347] Leveraging genome and phenome-wide association studies to investigate genetic risk of acute lymphoblastic leukemia.