rs8176785
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (A;A) | 0 |
| Make rs8176785(A;G) |
| Make rs8176785(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 11 |
| Position | 20783740 |
| Gene | NELL1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs8176785 |
| dbSNP (classic) | rs8176785 |
| ClinGen | rs8176785 |
| ebi | rs8176785 |
| HLI | rs8176785 |
| Exac | rs8176785 |
| Gnomad | rs8176785 |
| Varsome | rs8176785 |
| LitVar | rs8176785 |
| Map | rs8176785 |
| PheGenI | rs8176785 |
| Biobank | rs8176785 |
| 1000 genomes | rs8176785 |
| hgdp | rs8176785 |
| ensembl | rs8176785 |
| geneview | rs8176785 |
| scholar | rs8176785 |
| rs8176785 | |
| pharmgkb | rs8176785 |
| gwascentral | rs8176785 |
| openSNP | rs8176785 |
| 23andMe | rs8176785 |
| SNPshot | rs8176785 |
| SNPdbe | rs8176785 |
| MSV3d | rs8176785 |
| GWAS Ctlg | rs8176785 |
| GMAF | 0.3136 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 17684544
] Systematic association mapping identifies NELL1 as a novel IBD disease gene.
[PMID 22495925] Genetic polymorphisms inside and outside the MHC improve prediction of AS radiographic severity in addition to clinical variables.
