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rs910191

From SNPedia

Orientationminus
Stabilizedminus
Make rs910191(C;C)
Make rs910191(C;T)
Make rs910191(T;T)
ReferenceGRCh38 38.1/141
Chromosome20
Position48460486
is asnp
is mentioned by
dbSNPrs910191
ebirs910191
HLIrs910191
Exacrs910191
Varsomers910191
Maprs910191
PheGenIrs910191
hapmaprs910191
1000 genomesrs910191
hgdprs910191
ensemblrs910191
gopubmedrs910191
geneviewrs910191
scholarrs910191
googlers910191
pharmgkbrs910191
gwascentralrs910191
openSNPrs910191
23andMers910191
23andMe allrs910191
SNP Nexus

SNPshotrs910191
SNPdbers910191
MSV3drs910191
GWAS Ctlgrs910191
GMAF0.4004
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 23527680]
Trait Attention deficit hyperactivity disorder (combined symptoms)
Title Genome-wide association study of inattention and hyperactivity-impulsivity measured as quantitative traits.
Risk Allele A
P-val 2E-6
Odds Ratio NR NR