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rs5979785

From SNPedia

Orientationplus
Stabilizedplus
Make rs5979785(C;C)
Make rs5979785(C;T)
Make rs5979785(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position12953405
is asnp
is mentioned by
dbSNPrs5979785
ebirs5979785
HLIrs5979785
Exacrs5979785
Varsomers5979785
Maprs5979785
PheGenIrs5979785
hapmaprs5979785
1000 genomesrs5979785
hgdprs5979785
ensemblrs5979785
gopubmedrs5979785
geneviewrs5979785
scholarrs5979785
googlers5979785
pharmgkbrs5979785
gwascentralrs5979785
openSNPrs5979785
23andMers5979785
23andMe allrs5979785
SNP Nexus

SNPshotrs5979785
SNPdbers5979785
MSV3drs5979785
GWAS Ctlgrs5979785
GMAF0.4069
Max Magnitude
? (C;C) (C;T) (T;T) 28
[PMID 19956107OA-icon.png] Follow-up of 1715 SNPs from the Wellcome Trust Case Control Consortium genome-wide association study in type I diabetes families
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 6E-8
Odds Ratio 1.14 [1.09-1.19]


[PMID 19956109OA-icon.png] The Type I Diabetes Genetics Consortium 'Rapid Response' family-based candidate gene study: strategy, genes selection, and main outcome.