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rs6808138

From SNPedia

Orientationplus
Stabilizedplus
Make rs6808138(C;C)
Make rs6808138(C;G)
Make rs6808138(G;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position161674788
is asnp
is mentioned by
dbSNPrs6808138
ebirs6808138
HLIrs6808138
Exacrs6808138
Varsomers6808138
Maprs6808138
PheGenIrs6808138
hapmaprs6808138
1000 genomesrs6808138
hgdprs6808138
ensemblrs6808138
gopubmedrs6808138
geneviewrs6808138
scholarrs6808138
googlers6808138
pharmgkbrs6808138
gwascentralrs6808138
openSNPrs6808138
23andMers6808138
23andMe allrs6808138
SNP Nexus

SNPshotrs6808138
SNPdbers6808138
MSV3drs6808138
GWAS Ctlgrs6808138
GMAF0.2071
Max Magnitude
? (C;C) (C;G) (G;G) 28
GWAS snp
PMID [PMID 18821565]
Trait Hyperactive-impulsive symptoms
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 0.000008
Odds Ratio NR NR
GET Evidence
rs6808138
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.1875
summary