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rs1495465

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs1495465(G;T)
Make rs1495465(T;T)
ReferenceGRCh38 38.1/141
Chromosome14
Position57549696
is asnp
is mentioned by
dbSNPrs1495465
ebirs1495465
HLIrs1495465
Exacrs1495465
Varsomers1495465
Maprs1495465
PheGenIrs1495465
hapmaprs1495465
1000 genomesrs1495465
hgdprs1495465
ensemblrs1495465
gopubmedrs1495465
geneviewrs1495465
scholarrs1495465
googlers1495465
pharmgkbrs1495465
gwascentralrs1495465
openSNPrs1495465
23andMers1495465
23andMe allrs1495465
SNP Nexus

SNPshotrs1495465
SNPdbers1495465
MSV3drs1495465
GWAS Ctlgrs1495465
Max Magnitude0
? (G;G) (G;T) (T;T) 28

[PMID 19334001] Contribution of IL23R but not ATG16L1 to Crohn's disease susceptibility in Koreans