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rs1951082

From SNPedia

Orientationplus
Stabilizedplus
Make rs1951082(A;A)
Make rs1951082(A;T)
Make rs1951082(T;T)
ReferenceGRCh38 38.1/141
Chromosome14
Position26790837
GeneRP11-626P14.1
is asnp
is mentioned by
dbSNPrs1951082
ebirs1951082
HLIrs1951082
Exacrs1951082
Varsomers1951082
Maprs1951082
PheGenIrs1951082
hapmaprs1951082
1000 genomesrs1951082
hgdprs1951082
ensemblrs1951082
gopubmedrs1951082
geneviewrs1951082
scholarrs1951082
googlers1951082
pharmgkbrs1951082
gwascentralrs1951082
openSNPrs1951082
23andMers1951082
23andMe allrs1951082
SNP Nexus

SNPshotrs1951082
SNPdbers1951082
MSV3drs1951082
GWAS Ctlgrs1951082
GMAF0.4334
Max Magnitude
? (A;A) (A;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 T
P-val 0.000005
Odds Ratio NR NR



GET Evidence
rs1951082
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.460938
summary