rs13141
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs13141(A;A) |
| Make rs13141(A;G) |
| Make rs13141(G;G) |
| Reference | GRCh38.p7 38.3/149 |
| Chromosome | 12 |
| Position | 121318281 |
| Gene | ANAPC5 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs13141 |
| dbSNP (classic) | rs13141 |
| ClinGen | rs13141 |
| ebi | rs13141 |
| HLI | rs13141 |
| Exac | rs13141 |
| Gnomad | rs13141 |
| Varsome | rs13141 |
| LitVar | rs13141 |
| Map | rs13141 |
| PheGenI | rs13141 |
| Biobank | rs13141 |
| 1000 genomes | rs13141 |
| hgdp | rs13141 |
| ensembl | rs13141 |
| geneview | rs13141 |
| scholar | rs13141 |
| rs13141 | |
| pharmgkb | rs13141 |
| gwascentral | rs13141 |
| openSNP | rs13141 |
| 23andMe | rs13141 |
| SNPshot | rs13141 |
| SNPdbe | rs13141 |
| MSV3d | rs13141 |
| GWAS Ctlg | rs13141 |
| Max Magnitude | 0 |
[PMID 28146470
] Rare and low-frequency coding variants alter human adult height.
