rs114518130
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs114518130(A;A) |
| Make rs114518130(A;G) |
| Make rs114518130(G;G) |
| Reference | GRCh38.p7 38.3/150 |
| Chromosome | 4 |
| Position | 57047087 |
| Gene | IGFBP7 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs114518130 |
| dbSNP (old) | rs114518130 |
| ClinGen | rs114518130 |
| ebi | rs114518130 |
| HLI | rs114518130 |
| Exac | rs114518130 |
| Gnomad | rs114518130 |
| Varsome | rs114518130 |
| LitVar | rs114518130 |
| Map | rs114518130 |
| PheGenI | rs114518130 |
| Biobank | rs114518130 |
| 1000 genomes | rs114518130 |
| hgdp | rs114518130 |
| ensembl | rs114518130 |
| gopubmed | rs114518130 |
| geneview | rs114518130 |
| scholar | rs114518130 |
| rs114518130 | |
| pharmgkb | rs114518130 |
| gwascentral | rs114518130 |
| openSNP | rs114518130 |
| 23andMe | rs114518130 |
| 23andMe all | rs114518130 |
| SNPshot | rs114518130 |
| SNPdbe | rs114518130 |
| MSV3d | rs114518130 |
| GWAS Ctlg | rs114518130 |
| Max Magnitude |
[PMID 28763065
] Genome-wide association analysis identifies common variants influencing infant brain volumes.
