rs1061651
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs1061651(A;A) |
| Make rs1061651(A;G) |
| Make rs1061651(G;G) |
| Reference | GRCh38.p2 38.2/146 |
| Chromosome | 12 |
| Position | 114670556 |
| Gene | TBX3 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1061651 |
| ClinGen | rs1061651 |
| ebi | rs1061651 |
| HLI | rs1061651 |
| Exac | rs1061651 |
| Varsome | rs1061651 |
| Map | rs1061651 |
| PheGenI | rs1061651 |
| hapmap | rs1061651 |
| 1000 genomes | rs1061651 |
| hgdp | rs1061651 |
| ensembl | rs1061651 |
| gopubmed | rs1061651 |
| geneview | rs1061651 |
| scholar | rs1061651 |
| rs1061651 | |
| pharmgkb | rs1061651 |
| gwascentral | rs1061651 |
| openSNP | rs1061651 |
| 23andMe | rs1061651 |
| 23andMe all | rs1061651 |
| SNP Nexus | |
| SNPshot | rs1061651 |
| SNPdbe | rs1061651 |
| MSV3d | rs1061651 |
| GWAS Ctlg | rs1061651 |
| Max Magnitude |
[PMID 26920143
] Analysis of functional germline variants in APOBEC3 and driver genes on breast cancer risk in Moroccan study population.
| ClinVar | |
|---|---|
| Risk | rs1061651(G;G) |
| Alt | rs1061651(G;G) |
| Reference | rs1061651(A;A) |
| Significance | Non-pathogenic |
| Disease | Ulnar-mammary syndrome |
| Variation | info |
| Gene | TBX3 |
| CLNDBN | Ulnar-mammary syndrome |
| Reversed | 1 |
| HGVS | NC_000012.11:g.115108361T>C |
| CLNSRC | |
| CLNACC | RCV000319833.1, |
