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rs573872

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in complete genomics
Make rs573872(G;G)
Make rs573872(G;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position153754374
is asnp
is mentioned by
dbSNPrs573872
ebirs573872
HLIrs573872
Exacrs573872
Varsomers573872
Maprs573872
PheGenIrs573872
hapmaprs573872
1000 genomesrs573872
hgdprs573872
ensemblrs573872
gopubmedrs573872
geneviewrs573872
scholarrs573872
googlers573872
pharmgkbrs573872
gwascentralrs573872
openSNPrs573872
23andMers573872
23andMe allrs573872
SNP Nexus

SNPshotrs573872
SNPdbers573872
MSV3drs573872
GWAS Ctlgrs573872
GMAF0.2006
Max Magnitude0
? (G;G) (G;T) (T;T) 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 G
P-val 5E-14
Odds Ratio 1.37 [1.26-1.48]