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rs2062305

From SNPedia

Orientationplus
Stabilizedplus
Make rs2062305(A;A)
Make rs2062305(A;G)
Make rs2062305(G;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position42478744
is asnp
is mentioned by
dbSNPrs2062305
ebirs2062305
HLIrs2062305
Exacrs2062305
Varsomers2062305
Maprs2062305
PheGenIrs2062305
hapmaprs2062305
1000 genomesrs2062305
hgdprs2062305
ensemblrs2062305
gopubmedrs2062305
geneviewrs2062305
scholarrs2062305
googlers2062305
pharmgkbrs2062305
gwascentralrs2062305
openSNPrs2062305
23andMers2062305
23andMe allrs2062305
SNP Nexus

SNPshotrs2062305
SNPdbers2062305
MSV3drs2062305
GWAS Ctlgrs2062305
GMAF0.3783
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 21102463OA-icon.png]
Trait
Title Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci
Risk Allele G
P-val 5E-10
Odds Ratio 1.1000 [1.05-1.15]