rs876659460
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (T;T) | 0 | common in clinvar |
| Make rs876659460(G;G) |
| Make rs876659460(G;T) |
| Reference | GRCh38.p2 38.2/147 |
| Chromosome | 5 |
| Position | 112835109 |
| Gene | APC |
| is a | snp |
| is | mentioned by |
| dbSNP | rs876659460 |
| dbSNP (classic) | rs876659460 |
| ClinGen | rs876659460 |
| ebi | rs876659460 |
| HLI | rs876659460 |
| Exac | rs876659460 |
| Gnomad | rs876659460 |
| Varsome | rs876659460 |
| LitVar | rs876659460 |
| Map | rs876659460 |
| PheGenI | rs876659460 |
| Biobank | rs876659460 |
| 1000 genomes | rs876659460 |
| hgdp | rs876659460 |
| ensembl | rs876659460 |
| geneview | rs876659460 |
| scholar | rs876659460 |
| rs876659460 | |
| pharmgkb | rs876659460 |
| gwascentral | rs876659460 |
| openSNP | rs876659460 |
| 23andMe | rs876659460 |
| SNPshot | rs876659460 |
| SNPdbe | rs876659460 |
| MSV3d | rs876659460 |
| GWAS Ctlg | rs876659460 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs876659460(G;G) |
| Alt | rs876659460(G;G) |
| Reference | Rs876659460(T;T) |
| Significance | Probable-Pathogenic |
| Disease | Hereditary cancer-predisposing syndrome |
| Variation | info |
| Gene | APC |
| CLNDBN | Hereditary cancer-predisposing syndrome |
| Reversed | 0 |
| HGVS | NC_000005.9:g.112170806T>G |
| CLNSRC | |
| CLNACC | RCV000222920.1, |
