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rs701157

From SNPedia

Orientationplus
Stabilizedplus
Make rs701157(C;C)
Make rs701157(C;T)
Make rs701157(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position230539080
is asnp
is mentioned by
dbSNPrs701157
ebirs701157
HLIrs701157
Exacrs701157
Varsomers701157
Maprs701157
PheGenIrs701157
hapmaprs701157
1000 genomesrs701157
hgdprs701157
ensemblrs701157
gopubmedrs701157
geneviewrs701157
scholarrs701157
googlers701157
pharmgkbrs701157
gwascentralrs701157
openSNPrs701157
23andMers701157
23andMe allrs701157
SNP Nexus

SNPshotrs701157
SNPdbers701157
MSV3drs701157
GWAS Ctlgrs701157
GMAF0.4642
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 18951430]
Trait Attention-deficit/hyperactivity disorder and conduct disorder
Title Conduct disorder and ADHD: Evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study
Risk Allele C
P-val 0.000004
Odds Ratio NR NR



GET Evidence
rs701157
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.453125
summary