Have questions? Visit https://www.reddit.com/r/SNPedia

rs864643

From SNPedia

Orientationminus
Stabilizedminus
Make rs864643(C;C)
Make rs864643(C;T)
Make rs864643(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position39514089
GeneMOBP
is asnp
is mentioned by
dbSNPrs864643
ebirs864643
HLIrs864643
Exacrs864643
Varsomers864643
Maprs864643
PheGenIrs864643
hapmaprs864643
1000 genomesrs864643
hgdprs864643
ensemblrs864643
gopubmedrs864643
geneviewrs864643
scholarrs864643
googlers864643
pharmgkbrs864643
gwascentralrs864643
openSNPrs864643
23andMers864643
23andMe allrs864643
SNP Nexus

SNPshotrs864643
SNPdbers864643
MSV3drs864643
GWAS Ctlgrs864643
GMAF0.3085
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 18839057]
Trait Attention-deficit/hyperactivity disorder
Title Molecular genetics of adult ADHD: converging evidence from genome-wide association and extended pedigree linkage studies
Risk Allele
P-val 1E-8
Odds Ratio NR NR


[PMID 17357082OA-icon.png] Identification of a novel risk locus for progressive supranuclear palsy by a pooled genomewide scan of 500,288 single-nucleotide polymorphisms.


GET Evidence
rs864643
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.335938
summary