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rs2058660

From SNPedia

Orientationminus
Stabilizedplus
Make rs2058660(C;C)
Make rs2058660(C;T)
Make rs2058660(T;T)
ReferenceGRCh38 38.1/142
Chromosome2
Position102437989
GeneIL18RAP
is asnp
is mentioned by
dbSNPrs2058660
ebirs2058660
HLIrs2058660
Exacrs2058660
Varsomers2058660
Maprs2058660
PheGenIrs2058660
hapmaprs2058660
1000 genomesrs2058660
hgdprs2058660
ensemblrs2058660
gopubmedrs2058660
geneviewrs2058660
scholarrs2058660
googlers2058660
pharmgkbrs2058660
gwascentralrs2058660
openSNPrs2058660
23andMers2058660
23andMe allrs2058660
SNP Nexus

SNPshotrs2058660
SNPdbers2058660
MSV3drs2058660
GWAS Ctlgrs2058660
GMAF0.2778
Max Magnitude
? (C;C) (C;T) (T;T) 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 2E-12
Odds Ratio 1.1900 [1.14-1.26]


[PMID 23103228OA-icon.png] Identification of IL18RAP/IL18R1 and IL12B as leprosy risk genes demonstrates shared pathogenesis between inflammation and infectious diseases.