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rs1496770

From SNPedia

Orientationminus
Stabilizedminus
Make rs1496770(A;A)
Make rs1496770(A;G)
Make rs1496770(G;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position78629694
GeneMAGI2
is asnp
is mentioned by
dbSNPrs1496770
ebirs1496770
HLIrs1496770
Exacrs1496770
Varsomers1496770
Maprs1496770
PheGenIrs1496770
hapmaprs1496770
1000 genomesrs1496770
hgdprs1496770
ensemblrs1496770
gopubmedrs1496770
geneviewrs1496770
scholarrs1496770
googlers1496770
pharmgkbrs1496770
gwascentralrs1496770
openSNPrs1496770
23andMers1496770
23andMe allrs1496770
SNP Nexus

SNPshotrs1496770
SNPdbers1496770
MSV3drs1496770
GWAS Ctlgrs1496770
GMAF0.3802
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