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rs1487630

From SNPedia

Orientationminus
Stabilizedminus
Make rs1487630(A;A)
Make rs1487630(A;G)
Make rs1487630(G;G)
ReferenceGRCh38 38.1/141
Chromosome4
Position38334202
is asnp
is mentioned by
dbSNPrs1487630
ebirs1487630
HLIrs1487630
Exacrs1487630
Varsomers1487630
Maprs1487630
PheGenIrs1487630
hapmaprs1487630
1000 genomesrs1487630
hgdprs1487630
ensemblrs1487630
gopubmedrs1487630
geneviewrs1487630
scholarrs1487630
googlers1487630
pharmgkbrs1487630
gwascentralrs1487630
openSNPrs1487630
23andMers1487630
23andMe allrs1487630
SNP Nexus

SNPshotrs1487630
SNPdbers1487630
MSV3drs1487630
GWAS Ctlgrs1487630
GMAF0.1726
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 23266558]
Trait Crohn's disease
Title A Genome-Wide Association Study Identifies 2 Susceptibility Loci for Crohn's Disease in a Japanese Population.
Risk Allele T
P-val 1E-11
Odds Ratio 1.33 [1.22-1.44]