rs3769825
Orientation | minus |
Stabilized | minus |
Make rs3769825(C;C) |
Make rs3769825(C;T) |
Make rs3769825(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 2 |
Position | 201246657 |
Gene | CASP8 |
is a | snp |
is | mentioned by |
dbSNP | rs3769825 |
dbSNP (classic) | rs3769825 |
ClinGen | rs3769825 |
ebi | rs3769825 |
HLI | rs3769825 |
Exac | rs3769825 |
Gnomad | rs3769825 |
Varsome | rs3769825 |
LitVar | rs3769825 |
Map | rs3769825 |
PheGenI | rs3769825 |
Biobank | rs3769825 |
1000 genomes | rs3769825 |
hgdp | rs3769825 |
ensembl | rs3769825 |
geneview | rs3769825 |
scholar | rs3769825 |
rs3769825 | |
pharmgkb | rs3769825 |
gwascentral | rs3769825 |
openSNP | rs3769825 |
23andMe | rs3769825 |
SNPshot | rs3769825 |
SNPdbe | rs3769825 |
MSV3d | rs3769825 |
GWAS Ctlg | rs3769825 |
GMAF | 0.3898 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 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 | T |
P-val | 3E-9 |
Odds Ratio | 1.19 [1.12-1.25] |
[PMID 19318553] A breast cancer risk haplotype in the caspase-8 gene.
[PMID 19414860] Genetic variation in caspase genes and risk of non-Hodgkin lymphoma: a pooled analysis of 3 population-based case-control studies.
[PMID 19531679] Polymorphisms and haplotypes in the caspase-3, caspase-7, and caspase-8 genes and risk for endometrial cancer: a population-based, case-control study in a Chinese population.
[PMID 19938081] Altered transmission of HOX and apoptotic SNPs identify a potential common pathway for clubfoot.
[PMID 22843554] Association between CASP8 and CASP10 polymorphisms and toxicity outcomes with platinum-based chemotherapy in Chinese patients with non-small cell lung cancer.
- Is a snp
- In dbSNP
- SNPs on chromosome 2
- Has genotype
- Has population
- On chip 23andMe v1
- On chip 23andMe v2
- On chip 23andMe v3
- On chip 23andMe v4
- On chip Affy GenomeWide 6
- On chip Ancestry v2
- On chip FTDNA2
- On chip FTDNA
- On chip HumanOmni1Quad
- On chip Illumina Human 1M
- On chip 23andMe v5
- On chip Ancestry v2c
- On chip Ancestry v2d