rs76601225
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs76601225(A;A) |
| Make rs76601225(A;C) |
| Make rs76601225(C;C) |
| Reference | GRCh38.p2 38.2/144 |
| Chromosome | 5 |
| Position | 112811070 |
| Gene | APC |
| is a | snp |
| is | mentioned by |
| dbSNP | rs76601225 |
| dbSNP (classic) | rs76601225 |
| ClinGen | rs76601225 |
| ebi | rs76601225 |
| HLI | rs76601225 |
| Exac | rs76601225 |
| Gnomad | rs76601225 |
| Varsome | rs76601225 |
| LitVar | rs76601225 |
| Map | rs76601225 |
| PheGenI | rs76601225 |
| Biobank | rs76601225 |
| 1000 genomes | rs76601225 |
| hgdp | rs76601225 |
| ensembl | rs76601225 |
| geneview | rs76601225 |
| scholar | rs76601225 |
| rs76601225 | |
| pharmgkb | rs76601225 |
| gwascentral | rs76601225 |
| openSNP | rs76601225 |
| 23andMe | rs76601225 |
| SNPshot | rs76601225 |
| SNPdbe | rs76601225 |
| MSV3d | rs76601225 |
| GWAS Ctlg | rs76601225 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs76601225(C;C) |
| Alt | rs76601225(C;C) |
| Reference | rs76601225(A;A) |
| Significance | Other |
| Disease | Familial colorectal cancer |
| Variation | info |
| Gene | APC |
| CLNDBN | Familial colorectal cancer |
| Reversed | 0 |
| HGVS | NC_000005.9:g.112146767A>C |
| CLNSRC | |
| CLNACC | RCV000073532.1, |
