rs10763976
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs10763976(A;A) |
| Make rs10763976(A;G) |
| Make rs10763976(G;G) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 10 |
| Position | 34275364 |
| Gene | PARD3 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs10763976 |
| dbSNP (classic) | rs10763976 |
| ClinGen | rs10763976 |
| ebi | rs10763976 |
| HLI | rs10763976 |
| Exac | rs10763976 |
| Gnomad | rs10763976 |
| Varsome | rs10763976 |
| LitVar | rs10763976 |
| Map | rs10763976 |
| PheGenI | rs10763976 |
| Biobank | rs10763976 |
| 1000 genomes | rs10763976 |
| hgdp | rs10763976 |
| ensembl | rs10763976 |
| geneview | rs10763976 |
| scholar | rs10763976 |
| rs10763976 | |
| pharmgkb | rs10763976 |
| gwascentral | rs10763976 |
| openSNP | rs10763976 |
| 23andMe | rs10763976 |
| SNPshot | rs10763976 |
| SNPdbe | rs10763976 |
| MSV3d | rs10763976 |
| GWAS Ctlg | rs10763976 |
| GMAF | 0.3861 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 20096742] Intestinal barrier gene variants may not explain the increased levels of antigliadin antibodies, suggesting other mechanisms than altered permeability
[PMID 17989107] Associations with tight junction genes PARD3 and MAGI2 in Dutch patients point to a common barrier defect for coeliac disease and ulcerative colitis.
