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rs2160322

From SNPedia

Orientationplus
Stabilizedplus
Make rs2160322(C;C)
Make rs2160322(C;G)
Make rs2160322(G;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position78462650
GeneMAGI2
is asnp
is mentioned by
dbSNPrs2160322
ebirs2160322
HLIrs2160322
Exacrs2160322
Varsomers2160322
Maprs2160322
PheGenIrs2160322
hapmaprs2160322
1000 genomesrs2160322
hgdprs2160322
ensemblrs2160322
gopubmedrs2160322
geneviewrs2160322
scholarrs2160322
googlers2160322
pharmgkbrs2160322
gwascentralrs2160322
openSNPrs2160322
23andMers2160322
23andMe allrs2160322
SNP Nexus

SNPshotrs2160322
SNPdbers2160322
MSV3drs2160322
GWAS Ctlgrs2160322
GMAF0.4669
Max Magnitude
? (C;C) (C;G) (G;G) 28
[PMID 18720471OA-icon.png] MAGI2 genetic variation and inflammatory bowel disease.