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rs6750486

From SNPedia

Orientationplus
Stabilizedplus
Make rs6750486(C;C)
Make rs6750486(C;T)
Make rs6750486(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position35301852
is asnp
is mentioned by
dbSNPrs6750486
ebirs6750486
HLIrs6750486
Exacrs6750486
Varsomers6750486
Maprs6750486
PheGenIrs6750486
hapmaprs6750486
1000 genomesrs6750486
hgdprs6750486
ensemblrs6750486
gopubmedrs6750486
geneviewrs6750486
scholarrs6750486
googlers6750486
pharmgkbrs6750486
gwascentralrs6750486
openSNPrs6750486
23andMers6750486
23andMe allrs6750486
SNP Nexus

SNPshotrs6750486
SNPdbers6750486
MSV3drs6750486
GWAS Ctlgrs6750486
GMAF0.1313
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 20585324OA-icon.png]
Trait Conduct disorder (symptom count)
Title Genome-wide association study of conduct disorder symptomatology
Risk Allele
P-val 0.000006
Odds Ratio 0.10 [NR] unit increase