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rs2199161

From SNPedia

Orientationplus
Stabilizedplus
Make rs2199161(C;C)
Make rs2199161(C;G)
Make rs2199161(G;G)
ReferenceGRCh38 38.1/141
Chromosome5
Position72114529
GeneMAP1B
is asnp
is mentioned by
dbSNPrs2199161
ebirs2199161
HLIrs2199161
Exacrs2199161
Varsomers2199161
Maprs2199161
PheGenIrs2199161
hapmaprs2199161
1000 genomesrs2199161
hgdprs2199161
ensemblrs2199161
gopubmedrs2199161
geneviewrs2199161
scholarrs2199161
googlers2199161
pharmgkbrs2199161
gwascentralrs2199161
openSNPrs2199161
23andMers2199161
23andMe allrs2199161
SNP Nexus

SNPshotrs2199161
SNPdbers2199161
MSV3drs2199161
GWAS Ctlgrs2199161
GMAF0.287
Max Magnitude
? (C;C) (C;G) (G;G) 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 0.000002
Odds Ratio NR NR


GET Evidence
rs2199161
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.734375
summary