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rs1335515

From SNPedia

Orientationplus
Stabilizedplus
Make rs1335515(C;C)
Make rs1335515(C;T)
Make rs1335515(T;T)
ReferenceGRCh38 38.1/141
Chromosome14
Position57918647
is asnp
is mentioned by
dbSNPrs1335515
ebirs1335515
HLIrs1335515
Exacrs1335515
Varsomers1335515
Maprs1335515
PheGenIrs1335515
hapmaprs1335515
1000 genomesrs1335515
hgdprs1335515
ensemblrs1335515
gopubmedrs1335515
geneviewrs1335515
scholarrs1335515
googlers1335515
pharmgkbrs1335515
gwascentralrs1335515
openSNPrs1335515
23andMers1335515
23andMe allrs1335515
SNP Nexus

SNPshotrs1335515
SNPdbers1335515
MSV3drs1335515
GWAS Ctlgrs1335515
GMAF0.1492
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 0.000008
Odds Ratio NR NR


GET Evidence
rs1335515
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.125
summary