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rs10900020

From SNPedia

Orientationplus
Stabilizedplus
Make rs10900020(A;A)
Make rs10900020(A;T)
Make rs10900020(T;T)
ReferenceGRCh38 38.1/142
Chromosome10
Position44331749
GeneCXCL12
is asnp
is mentioned by
dbSNPrs10900020
dbSNP (classic)rs10900020
ClinGenrs10900020
ebirs10900020
HLIrs10900020
Exacrs10900020
Gnomadrs10900020
Varsomers10900020
LitVarrs10900020
Maprs10900020
PheGenIrs10900020
Biobankrs10900020
1000 genomesrs10900020
hgdprs10900020
ensemblrs10900020
geneviewrs10900020
scholarrs10900020
googlers10900020
pharmgkbrs10900020
gwascentralrs10900020
openSNPrs10900020
23andMers10900020
SNPshotrs10900020
SNPdbers10900020
MSV3drs10900020
GWAS Ctlgrs10900020
GMAF0.07713
Max Magnitude0
? (A;A) (A;T) (T;T) 28


GWAS snp
PMID [PMID 23212062OA-icon.png]
Trait Schizophrenia
Title Genome-wide association study of clinical dimensions of schizophrenia: polygenic effect on disorganized symptoms.
Risk Allele
P-val 3E-6
Odds Ratio .15 [NR] unit decrease