rs1049253
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs1049253(C;C) |
| Make rs1049253(C;T) |
| Make rs1049253(T;T) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 4 |
| Position | 184627797 |
| Gene | CASP3 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1049253 |
| dbSNP (classic) | rs1049253 |
| ClinGen | rs1049253 |
| ebi | rs1049253 |
| HLI | rs1049253 |
| Exac | rs1049253 |
| Gnomad | rs1049253 |
| Varsome | rs1049253 |
| LitVar | rs1049253 |
| Map | rs1049253 |
| PheGenI | rs1049253 |
| Biobank | rs1049253 |
| 1000 genomes | rs1049253 |
| hgdp | rs1049253 |
| ensembl | rs1049253 |
| geneview | rs1049253 |
| scholar | rs1049253 |
| rs1049253 | |
| pharmgkb | rs1049253 |
| gwascentral | rs1049253 |
| openSNP | rs1049253 |
| 23andMe | rs1049253 |
| SNPshot | rs1049253 |
| SNPdbe | rs1049253 |
| MSV3d | rs1049253 |
| GWAS Ctlg | rs1049253 |
| GMAF | 0.08861 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 23271051
] A functional variant at the miR-885-5p binding site of CASP3 confers risk of both index and second primary malignancies in patients with head and neck cancer
[PMID 18520591] Sequence variants in host cell factor C1 are associated with Meniere's disease.
[PMID 19938081] Altered transmission of HOX and apoptotic SNPs identify a potential common pathway for clubfoot.
