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rs11712165

From SNPedia

Orientationplus
Stabilizedplus
Make rs11712165(G;G)
Make rs11712165(G;T)
Make rs11712165(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position119399949
GeneARHGAP31
is asnp
is mentioned by
dbSNPrs11712165
ebirs11712165
HLIrs11712165
Exacrs11712165
Varsomers11712165
Maprs11712165
PheGenIrs11712165
hapmaprs11712165
1000 genomesrs11712165
hgdprs11712165
ensemblrs11712165
gopubmedrs11712165
geneviewrs11712165
scholarrs11712165
googlers11712165
pharmgkbrs11712165
gwascentralrs11712165
openSNPrs11712165
23andMers11712165
23andMe allrs11712165
SNP Nexus

SNPshotrs11712165
SNPdbers11712165
MSV3drs11712165
GWAS Ctlgrs11712165
GMAF0.3035
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 8E-9
Odds Ratio 1.13 [1.08-1.17]