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rs7705924

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in complete genomics
(G;G) 2.5 higher odds of Crohn's disease
Make rs7705924(A;G)
ReferenceGRCh38 38.1/141
Chromosome5
Position102611094
GeneLINC00492
is asnp
is mentioned by
dbSNPrs7705924
ebirs7705924
HLIrs7705924
Exacrs7705924
Varsomers7705924
Maprs7705924
PheGenIrs7705924
hapmaprs7705924
1000 genomesrs7705924
hgdprs7705924
ensemblrs7705924
gopubmedrs7705924
geneviewrs7705924
scholarrs7705924
googlers7705924
pharmgkbrs7705924
gwascentralrs7705924
openSNPrs7705924
23andMers7705924
23andMe allrs7705924
SNP Nexus

SNPshotrs7705924
SNPdbers7705924
MSV3drs7705924
GWAS Ctlgrs7705924
GMAF0.06015
Max Magnitude2.5
? (A;A) (A;G) (G;G) 28
[PMID 22412388OA-icon.png] A genome-wide scan of ashkenazi jewish Crohn's disease suggests novel susceptibility Loci.