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rs12727642

From SNPedia

Orientationplus
Stabilizedplus
Make rs12727642(A;A)
Make rs12727642(A;C)
Make rs12727642(C;C)
ReferenceGRCh38 38.1/141
Chromosome1
Position7986612
GenePARK7
is asnp
is mentioned by
dbSNPrs12727642
ebirs12727642
HLIrs12727642
Exacrs12727642
Varsomers12727642
Maprs12727642
PheGenIrs12727642
hapmaprs12727642
1000 genomesrs12727642
hgdprs12727642
ensemblrs12727642
gopubmedrs12727642
geneviewrs12727642
scholarrs12727642
googlers12727642
pharmgkbrs12727642
gwascentralrs12727642
openSNPrs12727642
23andMers12727642
23andMe allrs12727642
SNP Nexus

SNPshotrs12727642
SNPdbers12727642
MSV3drs12727642
GWAS Ctlgrs12727642
GMAF0.09734
Max Magnitude
? (A;A) (A;C) (C;C) 28
GWAS snp
PMID [PMID 20190752OA-icon.png]
Trait Celiac disease
Title Multiple common variants for celiac disease influencing immune gene expression
Risk Allele A
P-val 9E-8
Odds Ratio 1.14 [1.09-1.20]


[PMID 24871462] Coeliac disease-associated polymorphisms influence thymic gene expression