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

rs4923705

From SNPedia

Orientationplus
Stabilizedplus
Make rs4923705(A;A)
Make rs4923705(A;G)
Make rs4923705(G;G)
ReferenceGRCh38 38.1/141
Chromosome15
Position36001404
is asnp
is mentioned by
dbSNPrs4923705
dbSNP (classic)rs4923705
ClinGenrs4923705
ebirs4923705
HLIrs4923705
Exacrs4923705
Gnomadrs4923705
Varsomers4923705
LitVarrs4923705
Maprs4923705
PheGenIrs4923705
Biobankrs4923705
1000 genomesrs4923705
hgdprs4923705
ensemblrs4923705
geneviewrs4923705
scholarrs4923705
googlers4923705
pharmgkbrs4923705
gwascentralrs4923705
openSNPrs4923705
23andMers4923705
SNPshotrs4923705
SNPdbers4923705
MSV3drs4923705
GWAS Ctlgrs4923705
GMAF0.3563
Max Magnitude0
? (A;A) (A;G) (G;G) 28


GWAS snp
PMID [PMID 20732626OA-icon.png]
Trait
Title Family-Based Genome-Wide Association Scan of Attention-Deficit/Hyperactivity Disorder
Risk Allele C
P-val 0.000002
Odds Ratio 1.51 [NR]