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

rs2235356

From SNPedia

Orientationplus
Stabilizedplus
Make rs2235356(A;A)
Make rs2235356(A;G)
Make rs2235356(G;G)
ReferenceGRCh38 38.1/141
Chromosome22
Position50271920
GeneMAPK11
is asnp
is mentioned by
dbSNPrs2235356
ClinGenrs2235356
ebirs2235356
HLIrs2235356
Exacrs2235356
Varsomers2235356
Maprs2235356
PheGenIrs2235356
hapmaprs2235356
1000 genomesrs2235356
hgdprs2235356
ensemblrs2235356
gopubmedrs2235356
geneviewrs2235356
scholarrs2235356
googlers2235356
pharmgkbrs2235356
gwascentralrs2235356
openSNPrs2235356
23andMers2235356
23andMe allrs2235356
SNP Nexus

SNPshotrs2235356
SNPdbers2235356
MSV3drs2235356
GWAS Ctlgrs2235356
GMAF0.4151
Max Magnitude
? (A;A) (A;G) (G;G) 28
[PMID 23946768OA-icon.png] A genetic variation of the p38β promoter region is correlated with an increased risk of sporadic colorectal cancer