rs4986172
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs4986172(C;C) |
| Make rs4986172(C;T) |
| Make rs4986172(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 17 |
| Position | 45138914 |
| Gene | ACBD4 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs4986172 |
| dbSNP (classic) | rs4986172 |
| ClinGen | rs4986172 |
| ebi | rs4986172 |
| HLI | rs4986172 |
| Exac | rs4986172 |
| Gnomad | rs4986172 |
| Varsome | rs4986172 |
| LitVar | rs4986172 |
| Map | rs4986172 |
| PheGenI | rs4986172 |
| Biobank | rs4986172 |
| 1000 genomes | rs4986172 |
| hgdp | rs4986172 |
| ensembl | rs4986172 |
| geneview | rs4986172 |
| scholar | rs4986172 |
| rs4986172 | |
| pharmgkb | rs4986172 |
| gwascentral | rs4986172 |
| openSNP | rs4986172 |
| 23andMe | rs4986172 |
| SNPshot | rs4986172 |
| SNPdbe | rs4986172 |
| MSV3d | rs4986172 |
| GWAS Ctlg | rs4986172 |
| GMAF | 0.472 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 20881960 ]
|
| Trait | Height |
| Title | Hundreds of variants clustered in genomic loci and biological pathways affect human height |
| Risk Allele | T |
| P-val | 2E-16 |
| Odds Ratio | 0.03 [NR] unit decrease |
