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rs2769967

From SNPedia

Orientationplus
Stabilizedplus
Make rs2769967(C;C)
Make rs2769967(C;G)
Make rs2769967(G;G)
ReferenceGRCh38 38.1/141
Chromosome9
Position79274443
is asnp
is mentioned by
dbSNPrs2769967
ebirs2769967
HLIrs2769967
Exacrs2769967
Varsomers2769967
Maprs2769967
PheGenIrs2769967
hapmaprs2769967
1000 genomesrs2769967
hgdprs2769967
ensemblrs2769967
gopubmedrs2769967
geneviewrs2769967
scholarrs2769967
googlers2769967
pharmgkbrs2769967
gwascentralrs2769967
openSNPrs2769967
23andMers2769967
23andMe allrs2769967
SNP Nexus

SNPshotrs2769967
SNPdbers2769967
MSV3drs2769967
GWAS Ctlgrs2769967
GMAF0.4977
Max Magnitude
? (C;C) (C;G) (G;G) 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 0.000003
Odds Ratio NR NR


GET Evidence
rs2769967
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.5
summary