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

rs6719977

From SNPedia

Orientationplus
Stabilizedplus
Make rs6719977(C;C)
Make rs6719977(C;T)
Make rs6719977(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position42758663
is asnp
is mentioned by
dbSNPrs6719977
ebirs6719977
HLIrs6719977
Exacrs6719977
Varsomers6719977
Maprs6719977
PheGenIrs6719977
hapmaprs6719977
1000 genomesrs6719977
hgdprs6719977
ensemblrs6719977
gopubmedrs6719977
geneviewrs6719977
scholarrs6719977
googlers6719977
pharmgkbrs6719977
gwascentralrs6719977
openSNPrs6719977
23andMers6719977
23andMe allrs6719977
SNP Nexus

SNPshotrs6719977
SNPdbers6719977
MSV3drs6719977
GWAS Ctlgrs6719977
GMAF0.2994
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 18821565]
Trait Hyperactive-impulsive 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 0.000002
Odds Ratio NR NR


[PMID 20145962OA-icon.png] Molecular genetics of attention-deficit/hyperactivity disorder: an overview.


GET Evidence
rs6719977
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.632812
summary