rs414098
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs414098(A;A) |
| Make rs414098(A;G) |
| Make rs414098(G;G) |
| Reference | GRCh38.p2 38.2/144 |
| Chromosome | 5 |
| Position | 112778075 |
| Gene | APC |
| is a | snp |
| is | mentioned by |
| dbSNP | rs414098 |
| dbSNP (classic) | rs414098 |
| ClinGen | rs414098 |
| ebi | rs414098 |
| HLI | rs414098 |
| Exac | rs414098 |
| Gnomad | rs414098 |
| Varsome | rs414098 |
| LitVar | rs414098 |
| Map | rs414098 |
| PheGenI | rs414098 |
| Biobank | rs414098 |
| 1000 genomes | rs414098 |
| hgdp | rs414098 |
| ensembl | rs414098 |
| geneview | rs414098 |
| scholar | rs414098 |
| rs414098 | |
| pharmgkb | rs414098 |
| gwascentral | rs414098 |
| openSNP | rs414098 |
| 23andMe | rs414098 |
| SNPshot | rs414098 |
| SNPdbe | rs414098 |
| MSV3d | rs414098 |
| GWAS Ctlg | rs414098 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
| ClinVar | |
|---|---|
| Risk | rs414098(A;A) |
| Alt | rs414098(A;A) |
| Reference | rs414098(G;G) |
| Significance | Other |
| Disease | Familial colorectal cancer |
| Variation | info |
| Gene | APC |
| CLNDBN | Familial colorectal cancer |
| Reversed | 0 |
| HGVS | NC_000005.9:g.112113772G>A |
| CLNSRC | |
| CLNACC | RCV000073916.1, |
