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rs3892715

From SNPedia

Orientationplus
Stabilizedplus
Make rs3892715(C;C)
Make rs3892715(C;T)
Make rs3892715(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position195037281
is asnp
is mentioned by
dbSNPrs3892715
ebirs3892715
HLIrs3892715
Exacrs3892715
Varsomers3892715
Maprs3892715
PheGenIrs3892715
hapmaprs3892715
1000 genomesrs3892715
hgdprs3892715
ensemblrs3892715
gopubmedrs3892715
geneviewrs3892715
scholarrs3892715
googlers3892715
pharmgkbrs3892715
gwascentralrs3892715
openSNPrs3892715
23andMers3892715
23andMe allrs3892715
SNP Nexus

SNPshotrs3892715
SNPdbers3892715
MSV3drs3892715
GWAS Ctlgrs3892715
GMAF0.4931
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 C
P-val 0.000006
Odds Ratio NR NR


GET Evidence
rs3892715
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.5625
summary