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rs2605393

From SNPedia

Orientationplus
Stabilizedplus
Make rs2605393(G;G)
Make rs2605393(G;T)
Make rs2605393(T;T)
ReferenceGRCh38 38.1/142
Chromosome3
Position36368109
is asnp
is mentioned by
dbSNPrs2605393
ebirs2605393
HLIrs2605393
Exacrs2605393
Varsomers2605393
Maprs2605393
PheGenIrs2605393
hapmaprs2605393
1000 genomesrs2605393
hgdprs2605393
ensemblrs2605393
gopubmedrs2605393
geneviewrs2605393
scholarrs2605393
googlers2605393
pharmgkbrs2605393
gwascentralrs2605393
openSNPrs2605393
23andMers2605393
23andMe allrs2605393
SNP Nexus

SNPshotrs2605393
SNPdbers2605393
MSV3drs2605393
GWAS Ctlgrs2605393
Max Magnitude
? (G;G) (G;T) (T;T) 28
GWAS snp
PMID [PMID 23936387OA-icon.png]
Trait Celiac disease
Title A possible mechanism behind autoimmune disorders discovered by genome-wide linkage and association analysis in celiac disease.
Risk Allele G
P-val 6E-6
Odds Ratio NR NR