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rs1736148

From SNPedia

Orientationplus
Stabilizedplus
Make rs1736148(C;C)
Make rs1736148(C;T)
Make rs1736148(T;T)
ReferenceGRCh38 38.1/141
Chromosome21
Position15440893
GeneLOC101927745
is asnp
is mentioned by
dbSNPrs1736148
dbSNP (classic)rs1736148
ClinGenrs1736148
ebirs1736148
HLIrs1736148
Exacrs1736148
Gnomadrs1736148
Varsomers1736148
LitVarrs1736148
Maprs1736148
PheGenIrs1736148
Biobankrs1736148
1000 genomesrs1736148
hgdprs1736148
ensemblrs1736148
geneviewrs1736148
scholarrs1736148
googlers1736148
pharmgkbrs1736148
gwascentralrs1736148
openSNPrs1736148
23andMers1736148
23andMe allrs1736148
SNPshotrs1736148
SNPdbers1736148
MSV3drs1736148
GWAS Ctlgrs1736148
GMAF0.3926
Max Magnitude0
? (C;C) (C;T) (T;T) 28


DeCode reports that rs1736148 is associated with susceptibility to Crohn's disease. [PMID 18587394OA-icon.png]