rs2788612
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common genotype |
| Make rs2788612(C;T) |
| Make rs2788612(T;T) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 1 |
| Position | 111873741 |
| Gene | KCND3 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2788612 |
| dbSNP (classic) | rs2788612 |
| ClinGen | rs2788612 |
| ebi | rs2788612 |
| HLI | rs2788612 |
| Exac | rs2788612 |
| Gnomad | rs2788612 |
| Varsome | rs2788612 |
| LitVar | rs2788612 |
| Map | rs2788612 |
| PheGenI | rs2788612 |
| Biobank | rs2788612 |
| 1000 genomes | rs2788612 |
| hgdp | rs2788612 |
| ensembl | rs2788612 |
| geneview | rs2788612 |
| scholar | rs2788612 |
| rs2788612 | |
| pharmgkb | rs2788612 |
| gwascentral | rs2788612 |
| openSNP | rs2788612 |
| 23andMe | rs2788612 |
| SNPshot | rs2788612 |
| SNPdbe | rs2788612 |
| MSV3d | rs2788612 |
| GWAS Ctlg | rs2788612 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 24785509] |
| Trait | Response to radiotherapy in cancer (late toxicity) |
| Title | A genome wide association study (GWAS) providing evidence of an association between common genetic variants and late radiotherapy toxicity. |
| Risk Allele | |
| P-val | 6E-16 |
| Odds Ratio | .18 [NR] unit increase |
