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rs11712066

From SNPedia

Orientationplus
Stabilizedplus
Make rs11712066(A;A)
Make rs11712066(A;G)
Make rs11712066(G;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position152112520
is asnp
is mentioned by
dbSNPrs11712066
ebirs11712066
HLIrs11712066
Exacrs11712066
Varsomers11712066
Maprs11712066
PheGenIrs11712066
hapmaprs11712066
1000 genomesrs11712066
hgdprs11712066
ensemblrs11712066
gopubmedrs11712066
geneviewrs11712066
scholarrs11712066
googlers11712066
pharmgkbrs11712066
gwascentralrs11712066
openSNPrs11712066
23andMers11712066
23andMe allrs11712066
SNP Nexus

SNPshotrs11712066
SNPdbers11712066
MSV3drs11712066
GWAS Ctlgrs11712066
GMAF0.1019
Max Magnitude
? (A;A) (A;G) (G;G) 28
[PMID 22306654OA-icon.png] Common variants near MBNL1 and NKX2-5 are associated with infantile hypertrophic pyloric stenosis
GWAS snp
PMID [PMID 23989729OA-icon.png]
Trait Infantile hypertrophic pyloric stenosis
Title Plasma lipids, genetic variants near APOA1, and the risk of infantile hypertrophic pyloric stenosis.
Risk Allele A
P-val 3E-21
Odds Ratio 1.55 [1.42-1.70]