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rs1644305

From SNPedia

Orientationminus
Stabilizedminus
Make rs1644305(C;C)
Make rs1644305(C;T)
Make rs1644305(T;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position133867905
is asnp
is mentioned by
dbSNPrs1644305
ebirs1644305
HLIrs1644305
Exacrs1644305
Varsomers1644305
Maprs1644305
PheGenIrs1644305
hapmaprs1644305
1000 genomesrs1644305
hgdprs1644305
ensemblrs1644305
gopubmedrs1644305
geneviewrs1644305
scholarrs1644305
googlers1644305
pharmgkbrs1644305
gwascentralrs1644305
openSNPrs1644305
23andMers1644305
23andMe allrs1644305
SNP Nexus

SNPshotrs1644305
SNPdbers1644305
MSV3drs1644305
GWAS Ctlgrs1644305
GMAF0.3053
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 18951430]
Trait Attention-deficit/hyperactivity disorder and conduct disorder
Title Conduct disorder and ADHD: Evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study
Risk Allele A
P-val 0.000008
Odds Ratio NR NR



GET Evidence
rs1644305
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.367188
summary