rs11861007
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs11861007(C;C) |
| Make rs11861007(C;T) |
| Make rs11861007(T;T) |
| Reference | GRCh38.p7 38.3/150 |
| Chromosome | 16 |
| Position | 79204788 |
| Gene | MAF, WWOX |
| is a | snp |
| is | mentioned by |
| dbSNP | rs11861007 |
| dbSNP (classic) | rs11861007 |
| ClinGen | rs11861007 |
| ebi | rs11861007 |
| HLI | rs11861007 |
| Exac | rs11861007 |
| Gnomad | rs11861007 |
| Varsome | rs11861007 |
| LitVar | rs11861007 |
| Map | rs11861007 |
| PheGenI | rs11861007 |
| Biobank | rs11861007 |
| 1000 genomes | rs11861007 |
| hgdp | rs11861007 |
| ensembl | rs11861007 |
| geneview | rs11861007 |
| scholar | rs11861007 |
| rs11861007 | |
| pharmgkb | rs11861007 |
| gwascentral | rs11861007 |
| openSNP | rs11861007 |
| 23andMe | rs11861007 |
| SNPshot | rs11861007 |
| SNPdbe | rs11861007 |
| MSV3d | rs11861007 |
| GWAS Ctlg | rs11861007 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
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| ||
[PMID 29361163] Genomic and expression analyses identify a disease modifying variant for fibrostenotic Crohn's disease.
