rs7705924
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (A;A) | 0 | common in complete genomics |
| (G;G) | 2.5 | higher odds of Crohn's disease |
| Make rs7705924(A;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 5 |
| Position | 102611094 |
| Gene | LINC00491, LINC00492 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs7705924 |
| dbSNP (classic) | rs7705924 |
| ClinGen | rs7705924 |
| ebi | rs7705924 |
| HLI | rs7705924 |
| Exac | rs7705924 |
| Gnomad | rs7705924 |
| Varsome | rs7705924 |
| LitVar | rs7705924 |
| Map | rs7705924 |
| PheGenI | rs7705924 |
| Biobank | rs7705924 |
| 1000 genomes | rs7705924 |
| hgdp | rs7705924 |
| ensembl | rs7705924 |
| geneview | rs7705924 |
| scholar | rs7705924 |
| rs7705924 | |
| pharmgkb | rs7705924 |
| gwascentral | rs7705924 |
| openSNP | rs7705924 |
| 23andMe | rs7705924 |
| SNPshot | rs7705924 |
| SNPdbe | rs7705924 |
| MSV3d | rs7705924 |
| GWAS Ctlg | rs7705924 |
| GMAF | 0.06015 |
| Max Magnitude | 2.5 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 22412388
] A genome-wide scan of ashkenazi jewish Crohn's disease suggests novel susceptibility Loci.
