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rs1350666

From SNPedia

Orientationplus
Stabilizedplus
Make rs1350666(C;C)
Make rs1350666(C;T)
Make rs1350666(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position74358873
is asnp
is mentioned by
dbSNPrs1350666
ebirs1350666
HLIrs1350666
Exacrs1350666
Varsomers1350666
Maprs1350666
PheGenIrs1350666
hapmaprs1350666
1000 genomesrs1350666
hgdprs1350666
ensemblrs1350666
gopubmedrs1350666
geneviewrs1350666
scholarrs1350666
googlers1350666
pharmgkbrs1350666
gwascentralrs1350666
openSNPrs1350666
23andMers1350666
23andMe allrs1350666
SNP Nexus

SNPshotrs1350666
SNPdbers1350666
MSV3drs1350666
GWAS Ctlgrs1350666
GMAF0.3664
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 18821565]
Trait Attention deficit hyperactivity disorder
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
rs1350666
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.571429
summary