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rs17760268

From SNPedia

Orientationplus
Stabilizedplus
Make rs17760268(C;C)
Make rs17760268(C;T)
Make rs17760268(T;T)
ReferenceGRCh38 38.1/142
Chromosome17
Position56533930
is asnp
is mentioned by
dbSNPrs17760268
ebirs17760268
HLIrs17760268
Exacrs17760268
Varsomers17760268
Maprs17760268
PheGenIrs17760268
hapmaprs17760268
1000 genomesrs17760268
hgdprs17760268
ensemblrs17760268
gopubmedrs17760268
geneviewrs17760268
scholarrs17760268
googlers17760268
pharmgkbrs17760268
gwascentralrs17760268
openSNPrs17760268
23andMers17760268
23andMe allrs17760268
SNP Nexus

SNPshotrs17760268
SNPdbers17760268
MSV3drs17760268
GWAS Ctlgrs17760268
Max Magnitude
? (C;C) (C;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 C
P-val 4E-6
Odds Ratio NR NR