Have questions? Visit https://www.reddit.com/r/SNPedia

rs10487524

From SNPedia

Orientationminus
Stabilizedminus
Make rs10487524(C;C)
Make rs10487524(C;T)
Make rs10487524(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position145144438
is asnp
is mentioned by
dbSNPrs10487524
ebirs10487524
HLIrs10487524
Exacrs10487524
Varsomers10487524
Maprs10487524
PheGenIrs10487524
hapmaprs10487524
1000 genomesrs10487524
hgdprs10487524
ensemblrs10487524
gopubmedrs10487524
geneviewrs10487524
scholarrs10487524
googlers10487524
pharmgkbrs10487524
gwascentralrs10487524
openSNPrs10487524
23andMers10487524
23andMe allrs10487524
SNP Nexus

SNPshotrs10487524
SNPdbers10487524
MSV3drs10487524
GWAS Ctlgrs10487524
GMAF0.2277
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 T
P-val 0.000009
Odds Ratio 1.60 [NR]