rs71455793
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs71455793(A;A) |
| Make rs71455793(A;G) |
| Make rs71455793(G;G) |
| Reference | GRCh38.p7 38.3/149 |
| Chromosome | 11 |
| Position | 65947733 |
| Gene | TSGA10IP |
| is a | snp |
| is | mentioned by |
| dbSNP | rs71455793 |
| dbSNP (classic) | rs71455793 |
| ClinGen | rs71455793 |
| ebi | rs71455793 |
| HLI | rs71455793 |
| Exac | rs71455793 |
| Gnomad | rs71455793 |
| Varsome | rs71455793 |
| LitVar | rs71455793 |
| Map | rs71455793 |
| PheGenI | rs71455793 |
| Biobank | rs71455793 |
| 1000 genomes | rs71455793 |
| hgdp | rs71455793 |
| ensembl | rs71455793 |
| geneview | rs71455793 |
| scholar | rs71455793 |
| rs71455793 | |
| pharmgkb | rs71455793 |
| gwascentral | rs71455793 |
| openSNP | rs71455793 |
| 23andMe | rs71455793 |
| SNPshot | rs71455793 |
| SNPdbe | rs71455793 |
| MSV3d | rs71455793 |
| GWAS Ctlg | rs71455793 |
| Max Magnitude | 0 |
[PMID 28146470
] Rare and low-frequency coding variants alter human adult height.
