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rs1517484

From SNPedia

Orientationplus
Stabilizedplus
Make rs1517484(C;C)
Make rs1517484(C;T)
Make rs1517484(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position225373194
is asnp
is mentioned by
dbSNPrs1517484
ebirs1517484
HLIrs1517484
Exacrs1517484
Varsomers1517484
Maprs1517484
PheGenIrs1517484
hapmaprs1517484
1000 genomesrs1517484
hgdprs1517484
ensemblrs1517484
gopubmedrs1517484
geneviewrs1517484
scholarrs1517484
googlers1517484
pharmgkbrs1517484
gwascentralrs1517484
openSNPrs1517484
23andMers1517484
23andMe allrs1517484
SNP Nexus

SNPshotrs1517484
SNPdbers1517484
MSV3drs1517484
GWAS Ctlgrs1517484
GMAF0.388
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 5E-7
Odds Ratio NR NR


GET Evidence
rs1517484
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.359649
summary