rs116858574
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs116858574(C;C) |
| Make rs116858574(C;T) |
| Make rs116858574(T;T) |
| Reference | GRCh38.p7 38.3/149 |
| Chromosome | 15 |
| Position | 34228486 |
| Gene | EMC4 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs116858574 |
| dbSNP (classic) | rs116858574 |
| ClinGen | rs116858574 |
| ebi | rs116858574 |
| HLI | rs116858574 |
| Exac | rs116858574 |
| Gnomad | rs116858574 |
| Varsome | rs116858574 |
| LitVar | rs116858574 |
| Map | rs116858574 |
| PheGenI | rs116858574 |
| Biobank | rs116858574 |
| 1000 genomes | rs116858574 |
| hgdp | rs116858574 |
| ensembl | rs116858574 |
| geneview | rs116858574 |
| scholar | rs116858574 |
| rs116858574 | |
| pharmgkb | rs116858574 |
| gwascentral | rs116858574 |
| openSNP | rs116858574 |
| 23andMe | rs116858574 |
| SNPshot | rs116858574 |
| SNPdbe | rs116858574 |
| MSV3d | rs116858574 |
| GWAS Ctlg | rs116858574 |
| Max Magnitude | 0 |
[PMID 28146470
] Rare and low-frequency coding variants alter human adult height.
