Have questions? Visit https://www.reddit.com/r/SNPedia

rs7785088

From SNPedia

Orientationplus
Stabilizedplus
Make rs7785088(A;A)
Make rs7785088(A;G)
Make rs7785088(G;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position78692296
GeneMAGI2
is asnp
is mentioned by
dbSNPrs7785088
ebirs7785088
HLIrs7785088
Exacrs7785088
Varsomers7785088
Maprs7785088
PheGenIrs7785088
hapmaprs7785088
1000 genomesrs7785088
hgdprs7785088
ensemblrs7785088
gopubmedrs7785088
geneviewrs7785088
scholarrs7785088
googlers7785088
pharmgkbrs7785088
gwascentralrs7785088
openSNPrs7785088
23andMers7785088
23andMe allrs7785088
SNP Nexus

SNPshotrs7785088
SNPdbers7785088
MSV3drs7785088
GWAS Ctlgrs7785088
GMAF0.4155
Max Magnitude
? (A;A) (A;G) (G;G) 28
[PMID 18720471OA-icon.png] MAGI2 genetic variation and inflammatory bowel disease.