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rs13010713

From SNPedia

Orientationplus
Stabilizedplus
Make rs13010713(A;A)
Make rs13010713(A;G)
Make rs13010713(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position181131318
GeneAC104820.2
is asnp
is mentioned by
dbSNPrs13010713
ebirs13010713
HLIrs13010713
Exacrs13010713
Varsomers13010713
Maprs13010713
PheGenIrs13010713
hapmaprs13010713
1000 genomesrs13010713
hgdprs13010713
ensemblrs13010713
gopubmedrs13010713
geneviewrs13010713
scholarrs13010713
googlers13010713
pharmgkbrs13010713
gwascentralrs13010713
openSNPrs13010713
23andMers13010713
23andMe allrs13010713
SNP Nexus

SNPshotrs13010713
SNPdbers13010713
MSV3drs13010713
GWAS Ctlgrs13010713
GMAF0.4472
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 20190752OA-icon.png]
Trait Celiac disease
Title Multiple common variants for celiac disease influencing immune gene expression
Risk Allele G
P-val 5E-11
Odds Ratio 1.13 [1.09-1.18]