rs1049216
| Orientation | minus |
| Stabilized | minus |
| Make rs1049216(C;C) |
| Make rs1049216(C;T) |
| Make rs1049216(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 4 |
| Position | 184628935 |
| Gene | CASP3 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1049216 |
| dbSNP (classic) | rs1049216 |
| ClinGen | rs1049216 |
| ebi | rs1049216 |
| HLI | rs1049216 |
| Exac | rs1049216 |
| Gnomad | rs1049216 |
| Varsome | rs1049216 |
| LitVar | rs1049216 |
| Map | rs1049216 |
| PheGenI | rs1049216 |
| Biobank | rs1049216 |
| 1000 genomes | rs1049216 |
| hgdp | rs1049216 |
| ensembl | rs1049216 |
| geneview | rs1049216 |
| scholar | rs1049216 |
| rs1049216 | |
| pharmgkb | rs1049216 |
| gwascentral | rs1049216 |
| openSNP | rs1049216 |
| 23andMe | rs1049216 |
| SNPshot | rs1049216 |
| SNPdbe | rs1049216 |
| MSV3d | rs1049216 |
| GWAS Ctlg | rs1049216 |
| GMAF | 0.4036 |
| Max Magnitude | 0 |
[PMID 23765963] HuGE systematic review and meta-analysis demonstrate association of CASP-3 and CASP-7 genetic polymorphisms with cancer risk
[PMID 17071630] Genetic variants in caspase genes and susceptibility to non-Hodgkin lymphoma.
rs1049216 is a SNP that has been found to significantly decrease the Non-Hodgkin Lymphoma.
[PMID 18381704
] Caspase polymorphisms and genetic susceptibility to multiple myeloma.
[PMID 18520591] Sequence variants in host cell factor C1 are associated with Meniere's disease.
[PMID 18829519] CASP3 polymorphisms and risk of squamous cell carcinoma of the head and neck.
[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 28114230] Association of Casp3 microRNA Target Site (1049216) SNP With the Risk and Progress of Cervical Squamous Cell Carcinoma.
[PMID 28738811] Associations of genetic variation in CASP3 gene with noise-induced hearing loss in a Chinese population: a case-control study.
[PMID 29930809] Induction of the apoptotic pathway by oxidative stress in spontaneous preterm birth: Single nucleotide polymorphisms, maternal lifestyle factors and health status.
