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rs10011926

From SNPedia

Orientationplus
Stabilizedplus
Make rs10011926(C;C)
Make rs10011926(C;T)
Make rs10011926(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position110105771
GeneELOVL6
is asnp
is mentioned by
dbSNPrs10011926
ebirs10011926
HLIrs10011926
Exacrs10011926
Varsomers10011926
Maprs10011926
PheGenIrs10011926
hapmaprs10011926
1000 genomesrs10011926
hgdprs10011926
ensemblrs10011926
gopubmedrs10011926
geneviewrs10011926
scholarrs10011926
googlers10011926
pharmgkbrs10011926
gwascentralrs10011926
openSNPrs10011926
23andMers10011926
23andMe allrs10011926
SNP Nexus

SNPshotrs10011926
SNPdbers10011926
MSV3drs10011926
GWAS Ctlgrs10011926
GMAF0.3802
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 20732626OA-icon.png]
Trait
Title Family-Based Genome-Wide Association Scan of Attention-Deficit/Hyperactivity Disorder
Risk Allele
P-val 0.000008
Odds Ratio 1.49 [NR]