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rs13314993

From SNPedia

Orientationplus
Stabilizedplus
Make rs13314993(G;G)
Make rs13314993(G;T)
Make rs13314993(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position32973977
is asnp
is mentioned by
dbSNPrs13314993
ebirs13314993
HLIrs13314993
Exacrs13314993
Varsomers13314993
Maprs13314993
PheGenIrs13314993
hapmaprs13314993
1000 genomesrs13314993
hgdprs13314993
ensemblrs13314993
gopubmedrs13314993
geneviewrs13314993
scholarrs13314993
googlers13314993
pharmgkbrs13314993
gwascentralrs13314993
openSNPrs13314993
23andMers13314993
23andMe allrs13314993
SNP Nexus

SNPshotrs13314993
SNPdbers13314993
MSV3drs13314993
GWAS Ctlgrs13314993
GMAF0.4307
Max Magnitude
? (G;G) (G;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 C
P-val 3E-9
Odds Ratio 1.13 [1.08-1.17]