rs488087
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in clinvar |
| Make rs488087(C;T) |
| Make rs488087(T;T) |
| Reference | GRCh38.p2 38.2/144 |
| Chromosome | 9 |
| Position | 133071212 |
| Gene | CEL |
| is a | snp |
| is | mentioned by |
| dbSNP | rs488087 |
| dbSNP (classic) | rs488087 |
| ClinGen | rs488087 |
| ebi | rs488087 |
| HLI | rs488087 |
| Exac | rs488087 |
| Gnomad | rs488087 |
| Varsome | rs488087 |
| LitVar | rs488087 |
| Map | rs488087 |
| PheGenI | rs488087 |
| Biobank | rs488087 |
| 1000 genomes | rs488087 |
| hgdp | rs488087 |
| ensembl | rs488087 |
| geneview | rs488087 |
| scholar | rs488087 |
| rs488087 | |
| pharmgkb | rs488087 |
| gwascentral | rs488087 |
| openSNP | rs488087 |
| 23andMe | rs488087 |
| SNPshot | rs488087 |
| SNPdbe | rs488087 |
| MSV3d | rs488087 |
| GWAS Ctlg | rs488087 |
| Max Magnitude | 0 |
[PMID 26498142
] Rs488087 single nucleotide polymorphism as predictive risk factor for pancreatic cancers
| ClinVar | |
|---|---|
| Risk | rs488087(T;T) |
| Alt | rs488087(T;T) |
| Reference | Rs488087(C;C) |
| Significance | Probable-non-pathogenic |
| Disease | not specified |
| Variation | info |
| Gene | CEL |
| CLNDBN | not specified |
| Reversed | 0 |
| HGVS | NC_000009.11:g.135946599C>T |
| CLNSRC | |
| CLNACC | RCV000116657.2, |
