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

rs8047014

From SNPedia

Orientationplus
Stabilizedplus
Make rs8047014(A;A)
Make rs8047014(A;C)
Make rs8047014(C;C)
ReferenceGRCh38 38.1/141
Chromosome16
Position69101146
is asnp
is mentioned by
dbSNPrs8047014
ebirs8047014
HLIrs8047014
Exacrs8047014
Varsomers8047014
Maprs8047014
PheGenIrs8047014
hapmaprs8047014
1000 genomesrs8047014
hgdprs8047014
ensemblrs8047014
gopubmedrs8047014
geneviewrs8047014
scholarrs8047014
googlers8047014
pharmgkbrs8047014
gwascentralrs8047014
openSNPrs8047014
23andMers8047014
23andMe allrs8047014
SNP Nexus

SNPshotrs8047014
SNPdbers8047014
MSV3drs8047014
GWAS Ctlgrs8047014
GMAF0.3838
Max Magnitude
? (A;A) (A;C) (C;C) 28
GWAS snp
PMID [PMID 18821565]
Trait Attention deficit hyperactivity disorder
Title Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations
Risk Allele
P-val 0.000004
Odds Ratio NR NR


GET Evidence
rs8047014
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.570312
summary