rs735665
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common on affy axiom data |
Make rs735665(A;A) |
Make rs735665(A;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 11 |
Position | 123490689 |
Gene | GRAMD1B |
is a | snp |
is | mentioned by |
dbSNP | rs735665 |
dbSNP (classic) | rs735665 |
ClinGen | rs735665 |
ebi | rs735665 |
HLI | rs735665 |
Exac | rs735665 |
Gnomad | rs735665 |
Varsome | rs735665 |
LitVar | rs735665 |
Map | rs735665 |
PheGenI | rs735665 |
Biobank | rs735665 |
1000 genomes | rs735665 |
hgdp | rs735665 |
ensembl | rs735665 |
geneview | rs735665 |
scholar | rs735665 |
rs735665 | |
pharmgkb | rs735665 |
gwascentral | rs735665 |
openSNP | rs735665 |
23andMe | rs735665 |
SNPshot | rs735665 |
SNPdbe | rs735665 |
MSV3d | rs735665 |
GWAS Ctlg | rs735665 |
GMAF | 0.1074 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
23andMe blog chronic lymphocytic leukemia
- rs735665 A 1.45
news Slager and colleagues validated these in an independent sample of patients. The strongest association was for rs735665 on 11q24, where the risk was 50 percent higher. This was closely followed by a 39 percent increased risk associated with rs9378805 on 6p25.
GWAS | |
---|---|
SNP | rs735665 |
PubMedID | [PMID 18758461] |
Condition | Chronic lymphocytic leukemia |
Gene | GRAMD1B |
Risk Allele | A |
pValue | 4.00E-012 |
OR | 1.45 |
95% CI | 1.31-1.61 |
[PMID 20332261] Genetic Susceptibility Variants for Chronic Lymphocytic Leukemia
GWAS snp | |
---|---|
PMID | [PMID 20639881] |
Trait | Follicular lymphoma |
Title | Genome-wide association study of follicular lymphoma identifies a risk locus at 6p21.32 |
Risk Allele | T |
P-val | 4E-9 |
Odds Ratio | 1.81 [1.50-2.20] |
[PMID 20855867] Inherited genetic susceptibility to monoclonal B-cell lymphocytosis
[PMID 19620980] Genetic variants at 6p21.33 are associated with susceptibility to follicular lymphoma.
[PMID 20731705] Genetic susceptibility for chronic lymphocytic leukemia among Chinese in Hong Kong.
GWAS snp | |
---|---|
PMID | [PMID 22700719] |
Trait | |
Title | Common variation at 6p21.31 (BAK1) influences the risk of chronic lymphocytic leukemia. |
Risk Allele | A |
P-val | 3E-12 |
Odds Ratio | 1.5200 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 | A |
P-val | 4E-39 |
Odds Ratio | 1.62 [NR] |
[PMID 23455380] Risk of genome-wide association study-identified genetic variants for non-Hodgkin lymphoma in a Chinese population.
GWAS snp | |
---|---|
PMID | [PMID 24292274] |
Trait | Chronic lymphocytic leukemia |
Title | A genome-wide association study identifies multiple susceptibility loci for chronic lymphocytic leukemia. |
Risk Allele | A |
P-val | 4E-24 |
Odds Ratio | 1.64 [NR] |
[PMID 29547969] A genome-wide association study of IgM antibody against phosphorylcholine: shared genetics and phenotypic relation to chronic lymphocytic leukemia.
- Is a snp
- In dbSNP
- SNPs on chromosome 11
- Has genotype
- Has population
- GWAS
- Uses omim
- On chip 23andMe v1
- On chip 23andMe v2
- On chip 23andMe v3
- On chip 23andMe v4
- On chip 23andMe v5
- On chip Affy GenomeWide 6
- On chip Affy500k
- On chip Ancestry v2
- On chip HumanOmni1Quad
- On chip Illumina Human 1M
- On chip Ancestry v2c
- On chip Ancestry v2d