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rs6427356

From SNPedia

Orientationplus
Stabilizedplus
Make rs6427356(A;A)
Make rs6427356(A;G)
Make rs6427356(G;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position157160775
is asnp
is mentioned by
dbSNPrs6427356
ebirs6427356
HLIrs6427356
Exacrs6427356
Varsomers6427356
Maprs6427356
PheGenIrs6427356
hapmaprs6427356
1000 genomesrs6427356
hgdprs6427356
ensemblrs6427356
gopubmedrs6427356
geneviewrs6427356
scholarrs6427356
googlers6427356
pharmgkbrs6427356
gwascentralrs6427356
openSNPrs6427356
23andMers6427356
23andMe allrs6427356
SNP Nexus

SNPshotrs6427356
SNPdbers6427356
MSV3drs6427356
GWAS Ctlgrs6427356
GMAF0.4793
Max Magnitude
? (A;A) (A;G) (G;G) 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 G
P-val 0.000008
Odds Ratio NR NR



GET Evidence
rs6427356
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.4375
summary