rs114233776
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs114233776(A;A) |
| Make rs114233776(A;G) |
| Make rs114233776(G;G) |
| Reference | GRCh38.p7 38.3/149 |
| Chromosome | 1 |
| Position | 41152625 |
| Gene | SCMH1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs114233776 |
| dbSNP (classic) | rs114233776 |
| ClinGen | rs114233776 |
| ebi | rs114233776 |
| HLI | rs114233776 |
| Exac | rs114233776 |
| Gnomad | rs114233776 |
| Varsome | rs114233776 |
| LitVar | rs114233776 |
| Map | rs114233776 |
| PheGenI | rs114233776 |
| Biobank | rs114233776 |
| 1000 genomes | rs114233776 |
| hgdp | rs114233776 |
| ensembl | rs114233776 |
| geneview | rs114233776 |
| scholar | rs114233776 |
| rs114233776 | |
| pharmgkb | rs114233776 |
| gwascentral | rs114233776 |
| openSNP | rs114233776 |
| 23andMe | rs114233776 |
| SNPshot | rs114233776 |
| SNPdbe | rs114233776 |
| MSV3d | rs114233776 |
| GWAS Ctlg | rs114233776 |
| Max Magnitude | 0 |
[PMID 28146470
] Rare and low-frequency coding variants alter human adult height.
