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rs11693697

From SNPedia

Orientationplus
Stabilizedplus
Make rs11693697(C;C)
Make rs11693697(C;T)
Make rs11693697(T;T)
ReferenceGRCh38 38.1/142
Chromosome2
Position102299202
is asnp
is mentioned by
dbSNPrs11693697
ebirs11693697
HLIrs11693697
Exacrs11693697
Varsomers11693697
Maprs11693697
PheGenIrs11693697
hapmaprs11693697
1000 genomesrs11693697
hgdprs11693697
ensemblrs11693697
gopubmedrs11693697
geneviewrs11693697
scholarrs11693697
googlers11693697
pharmgkbrs11693697
gwascentralrs11693697
openSNPrs11693697
23andMers11693697
23andMe allrs11693697
SNP Nexus

SNPshotrs11693697
SNPdbers11693697
MSV3drs11693697
GWAS Ctlgrs11693697
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 23999434OA-icon.png]
Trait Serum protein levels (sST2)
Title Common genetic variation at the IL1RL1 locus regulates IL-33/ST2 signaling.
Risk Allele C
P-val 7E-11
Odds Ratio .08 [0.06-0.1] unit decrease