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

rs17658378

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common on affy axiom data
Make rs17658378(A;G)
Make rs17658378(G;G)
ReferenceGRCh38 38.1/141
Chromosome8
Position115381846
is asnp
is mentioned by
dbSNPrs17658378
ebirs17658378
HLIrs17658378
Exacrs17658378
Varsomers17658378
Maprs17658378
PheGenIrs17658378
hapmaprs17658378
1000 genomesrs17658378
hgdprs17658378
ensemblrs17658378
gopubmedrs17658378
geneviewrs17658378
scholarrs17658378
googlers17658378
pharmgkbrs17658378
gwascentralrs17658378
openSNPrs17658378
23andMers17658378
23andMe allrs17658378
SNP Nexus

SNPshotrs17658378
SNPdbers17658378
MSV3drs17658378
GWAS Ctlgrs17658378
GMAF0.05647
Max Magnitude0
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 18937294OA-icon.png]
Trait Attention deficit hyperactivity disorder (time to onset)
Title Genome-wide association scan of the time to onset of attention deficit hyperactivity disorder
Risk Allele A
P-val 0.000009
Odds Ratio NR NR


GET Evidence
rs17658378
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.0546875
summary