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rs6968385

From SNPedia

Orientationplus
Stabilizedplus
Make rs6968385(C;C)
Make rs6968385(C;T)
Make rs6968385(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position110407414
is asnp
is mentioned by
dbSNPrs6968385
ebirs6968385
HLIrs6968385
Exacrs6968385
Varsomers6968385
Maprs6968385
PheGenIrs6968385
hapmaprs6968385
1000 genomesrs6968385
hgdprs6968385
ensemblrs6968385
gopubmedrs6968385
geneviewrs6968385
scholarrs6968385
googlers6968385
pharmgkbrs6968385
gwascentralrs6968385
openSNPrs6968385
23andMers6968385
23andMe allrs6968385
SNP Nexus

SNPshotrs6968385
SNPdbers6968385
MSV3drs6968385
GWAS Ctlgrs6968385
GMAF0.477
Max Magnitude
? (C;C) (C;T) (T;T) 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 T
P-val 0.000002
Odds Ratio NR NR


GET Evidence
rs6968385
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.507812
summary