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.
] 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.
] 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.
] 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.
] 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.
] 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


