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rs6962966

From SNPedia

Orientationplus
Stabilizedplus
Make rs6962966(A;A)
Make rs6962966(A;G)
Make rs6962966(G;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position78174806
GeneMAGI2
is asnp
is mentioned by
dbSNPrs6962966
ebirs6962966
HLIrs6962966
Exacrs6962966
Varsomers6962966
Maprs6962966
PheGenIrs6962966
hapmaprs6962966
1000 genomesrs6962966
hgdprs6962966
ensemblrs6962966
gopubmedrs6962966
geneviewrs6962966
scholarrs6962966
googlers6962966
pharmgkbrs6962966
gwascentralrs6962966
openSNPrs6962966
23andMers6962966
23andMe allrs6962966
SNP Nexus

SNPshotrs6962966
SNPdbers6962966
MSV3drs6962966
GWAS Ctlgrs6962966
GMAF0.4637
Max Magnitude
? (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.


[PMID 18720471OA-icon.png] MAGI2 genetic variation and inflammatory bowel disease.