rs143365597
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs143365597(A;A) |
| Make rs143365597(A;G) |
| Make rs143365597(G;G) |
| Reference | GRCh38.p7 38.3/149 |
| Chromosome | 1 |
| Position | 41075230 |
| Gene | SCMH1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs143365597 |
| dbSNP (classic) | rs143365597 |
| ClinGen | rs143365597 |
| ebi | rs143365597 |
| HLI | rs143365597 |
| Exac | rs143365597 |
| Gnomad | rs143365597 |
| Varsome | rs143365597 |
| LitVar | rs143365597 |
| Map | rs143365597 |
| PheGenI | rs143365597 |
| Biobank | rs143365597 |
| 1000 genomes | rs143365597 |
| hgdp | rs143365597 |
| ensembl | rs143365597 |
| geneview | rs143365597 |
| scholar | rs143365597 |
| rs143365597 | |
| pharmgkb | rs143365597 |
| gwascentral | rs143365597 |
| openSNP | rs143365597 |
| 23andMe | rs143365597 |
| SNPshot | rs143365597 |
| SNPdbe | rs143365597 |
| MSV3d | rs143365597 |
| GWAS Ctlg | rs143365597 |
| Max Magnitude | 0 |
[PMID 28146470
] Rare and low-frequency coding variants alter human adult height.
