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rs10858396

From SNPedia

Orientationplus
Stabilizedplus
Make rs10858396(A;A)
Make rs10858396(A;G)
Make rs10858396(G;G)
ReferenceGRCh38 38.1/141
Chromosome9
Position135383930
is asnp
is mentioned by
dbSNPrs10858396
ebirs10858396
HLIrs10858396
Exacrs10858396
Varsomers10858396
Maprs10858396
PheGenIrs10858396
hapmaprs10858396
1000 genomesrs10858396
hgdprs10858396
ensemblrs10858396
gopubmedrs10858396
geneviewrs10858396
scholarrs10858396
googlers10858396
pharmgkbrs10858396
gwascentralrs10858396
openSNPrs10858396
23andMers10858396
23andMe allrs10858396
SNP Nexus

SNPshotrs10858396
SNPdbers10858396
MSV3drs10858396
GWAS Ctlgrs10858396
GMAF0.259
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 21784300OA-icon.png]
Trait
Title Genome-wide association study of the child behavior checklist dysregulation profile.
Risk Allele
P-val 0.000006
Odds Ratio None None