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rs4650135

From SNPedia

Orientationplus
Stabilizedplus
Make rs4650135(C;C)
Make rs4650135(C;T)
Make rs4650135(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position69219314
is asnp
is mentioned by
dbSNPrs4650135
ebirs4650135
HLIrs4650135
Exacrs4650135
Varsomers4650135
Maprs4650135
PheGenIrs4650135
hapmaprs4650135
1000 genomesrs4650135
hgdprs4650135
ensemblrs4650135
gopubmedrs4650135
geneviewrs4650135
scholarrs4650135
googlers4650135
pharmgkbrs4650135
gwascentralrs4650135
openSNPrs4650135
23andMers4650135
23andMe allrs4650135
SNP Nexus

SNPshotrs4650135
SNPdbers4650135
MSV3drs4650135
GWAS Ctlgrs4650135
GMAF0.2571
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 18821565]
Trait Inattentive symptoms
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 0.000005
Odds Ratio NR NR


GET Evidence
rs4650135
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.242188
summary