rs11994014
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs11994014(A;A) |
| Make rs11994014(A;G) |
| Make rs11994014(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 8 |
| Position | 24944767 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs11994014 |
| dbSNP (classic) | rs11994014 |
| ClinGen | rs11994014 |
| ebi | rs11994014 |
| HLI | rs11994014 |
| Exac | rs11994014 |
| Gnomad | rs11994014 |
| Varsome | rs11994014 |
| LitVar | rs11994014 |
| Map | rs11994014 |
| PheGenI | rs11994014 |
| Biobank | rs11994014 |
| 1000 genomes | rs11994014 |
| hgdp | rs11994014 |
| ensembl | rs11994014 |
| geneview | rs11994014 |
| scholar | rs11994014 |
| rs11994014 | |
| pharmgkb | rs11994014 |
| gwascentral | rs11994014 |
| openSNP | rs11994014 |
| 23andMe | rs11994014 |
| SNPshot | rs11994014 |
| SNPdbe | rs11994014 |
| MSV3d | rs11994014 |
| GWAS Ctlg | rs11994014 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 25312269
] Common genetic variants in NEFL influence gene expression and neuroblastoma risk
