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rs8179116

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs8179116(A;A)
Make rs8179116(A;G)
ReferenceGRCh38 38.1/142
Chromosome12
Position108631651
GeneSELPLG
is asnp
is mentioned by
dbSNPrs8179116
ebirs8179116
HLIrs8179116
Exacrs8179116
Varsomers8179116
Maprs8179116
PheGenIrs8179116
hapmaprs8179116
1000 genomesrs8179116
hgdprs8179116
ensemblrs8179116
gopubmedrs8179116
geneviewrs8179116
scholarrs8179116
googlers8179116
pharmgkbrs8179116
gwascentralrs8179116
openSNPrs8179116
23andMers8179116
23andMe allrs8179116
SNP Nexus

SNPshotrs8179116
SNPdbers8179116
MSV3drs8179116
GWAS Ctlgrs8179116
GMAF0.02296
Max Magnitude0
? (A;A) (A;G) (G;G) 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 0.000003
Odds Ratio 0.23 [NR] unit increase