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rs8041675

From SNPedia

Orientationplus
Stabilizedplus
Make rs8041675(C;C)
Make rs8041675(C;T)
Make rs8041675(T;T)
ReferenceGRCh38 38.1/141
Chromosome15
Position37050401
GeneMEIS2
is asnp
is mentioned by
dbSNPrs8041675
ebirs8041675
HLIrs8041675
Exacrs8041675
Varsomers8041675
Maprs8041675
PheGenIrs8041675
hapmaprs8041675
1000 genomesrs8041675
hgdprs8041675
ensemblrs8041675
gopubmedrs8041675
geneviewrs8041675
scholarrs8041675
googlers8041675
pharmgkbrs8041675
gwascentralrs8041675
openSNPrs8041675
23andMers8041675
23andMe allrs8041675
SNP Nexus

SNPshotrs8041675
SNPdbers8041675
MSV3drs8041675
GWAS Ctlgrs8041675
GMAF0.4467
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 0.000004
Odds Ratio NR NR


GET Evidence
rs8041675
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.515625
summary