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rs11096990

From SNPedia

Orientationplus
Stabilizedplus
Make rs11096990(C;C)
Make rs11096990(C;T)
Make rs11096990(T;T)
ReferenceGRCh38 38.1/142
Chromosome4
Position39285329
GeneWDR19
is asnp
is mentioned by
dbSNPrs11096990
ebirs11096990
HLIrs11096990
Exacrs11096990
Varsomers11096990
Maprs11096990
PheGenIrs11096990
hapmaprs11096990
1000 genomesrs11096990
hgdprs11096990
ensemblrs11096990
gopubmedrs11096990
geneviewrs11096990
scholarrs11096990
googlers11096990
pharmgkbrs11096990
gwascentralrs11096990
openSNPrs11096990
23andMers11096990
23andMe allrs11096990
SNP Nexus

SNPshotrs11096990
SNPdbers11096990
MSV3drs11096990
GWAS Ctlgrs11096990
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 24684796OA-icon.png]
Trait Cognitive function
Title Heritability and genetic association analysis of cognition in the Diabetes Heart Study.
Risk Allele T
P-val 6E-7
Odds Ratio 2.01 [1.23-2.79] unit decrease