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rs29784

From SNPedia

Orientationminus
Stabilizedminus
Make rs29784(A;A)
Make rs29784(A;G)
Make rs29784(G;G)
ReferenceGRCh38 38.1/141
Chromosome5
Position173168305
is asnp
is mentioned by
dbSNPrs29784
ebirs29784
HLIrs29784
Exacrs29784
Varsomers29784
Maprs29784
PheGenIrs29784
hapmaprs29784
1000 genomesrs29784
hgdprs29784
ensemblrs29784
gopubmedrs29784
geneviewrs29784
scholarrs29784
googlers29784
pharmgkbrs29784
gwascentralrs29784
openSNPrs29784
23andMers29784
23andMe allrs29784
SNP Nexus

SNPshotrs29784
SNPdbers29784
MSV3drs29784
GWAS Ctlgrs29784
GMAF0.3512
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 T
P-val 8E-18
Odds Ratio 1.36 [1.27-1.46]