rs348601
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs348601(A;A) |
| Make rs348601(A;G) |
| Make rs348601(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 5 |
| Position | 40319904 |
| Gene | LOC105374736 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs348601 |
| dbSNP (classic) | rs348601 |
| ClinGen | rs348601 |
| ebi | rs348601 |
| HLI | rs348601 |
| Exac | rs348601 |
| Gnomad | rs348601 |
| Varsome | rs348601 |
| LitVar | rs348601 |
| Map | rs348601 |
| PheGenI | rs348601 |
| Biobank | rs348601 |
| 1000 genomes | rs348601 |
| hgdp | rs348601 |
| ensembl | rs348601 |
| geneview | rs348601 |
| scholar | rs348601 |
| rs348601 | |
| pharmgkb | rs348601 |
| gwascentral | rs348601 |
| openSNP | rs348601 |
| 23andMe | rs348601 |
| SNPshot | rs348601 |
| SNPdbe | rs348601 |
| MSV3d | rs348601 |
| GWAS Ctlg | rs348601 |
| GMAF | 0.477 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
rs348601 increases susceptibility to Crohn's disease 1.36 times for carriers of the A allele [PMID 17447842
]
