rs504963
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs504963(C;C) |
| Make rs504963(C;T) |
| Make rs504963(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 19 |
| Position | 48705608 |
| Gene | FUT2, LOC105447645, MAMSTR |
| is a | snp |
| is | mentioned by |
| dbSNP | rs504963 |
| dbSNP (classic) | rs504963 |
| ClinGen | rs504963 |
| ebi | rs504963 |
| HLI | rs504963 |
| Exac | rs504963 |
| Gnomad | rs504963 |
| Varsome | rs504963 |
| LitVar | rs504963 |
| Map | rs504963 |
| PheGenI | rs504963 |
| Biobank | rs504963 |
| 1000 genomes | rs504963 |
| hgdp | rs504963 |
| ensembl | rs504963 |
| geneview | rs504963 |
| scholar | rs504963 |
| rs504963 | |
| pharmgkb | rs504963 |
| gwascentral | rs504963 |
| openSNP | rs504963 |
| 23andMe | rs504963 |
| SNPshot | rs504963 |
| SNPdbe | rs504963 |
| MSV3d | rs504963 |
| GWAS Ctlg | rs504963 |
| GMAF | 0.3416 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 20570966 ]
|
| Trait | Crohn's disease |
| Title | Fucosyltransferase 2(FUT2) Non-Secretor Status is associated with Crohn's Disease |
| Risk Allele | A |
| P-val | 2E-8 |
| Odds Ratio | None None |
[PMID 18997004] Widespread balancing selection and pathogen-driven selection at blood group antigen genes.
[PMID 20041166] Common genetic variation and the control of HIV-1 in humans.
