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rs1250552

From SNPedia

Orientationminus
Stabilizedminus
Make rs1250552(C;C)
Make rs1250552(C;T)
Make rs1250552(T;T)
ReferenceGRCh38 38.1/142
Chromosome10
Position79298270
GeneZMIZ1
is asnp
is mentioned by
dbSNPrs1250552
ebirs1250552
HLIrs1250552
Exacrs1250552
Varsomers1250552
Maprs1250552
PheGenIrs1250552
hapmaprs1250552
1000 genomesrs1250552
hgdprs1250552
ensemblrs1250552
gopubmedrs1250552
geneviewrs1250552
scholarrs1250552
googlers1250552
pharmgkbrs1250552
gwascentralrs1250552
openSNPrs1250552
23andMers1250552
23andMe allrs1250552
SNP Nexus

SNPshotrs1250552
SNPdbers1250552
MSV3drs1250552
GWAS Ctlgrs1250552
GMAF0.4197
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 20190752OA-icon.png]
Trait Celiac disease
Title Multiple common variants for celiac disease influencing immune gene expression
Risk Allele
P-val 9E-10
Odds Ratio 1.12 [1.09-1.16]