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rs2910032

From SNPedia

Orientationplus
Stabilizedplus
Make rs2910032(C;C)
Make rs2910032(C;T)
Make rs2910032(T;T)
ReferenceGRCh38 38.1/142
Chromosome5
Position153160794
is asnp
is mentioned by
dbSNPrs2910032
ebirs2910032
HLIrs2910032
Exacrs2910032
Varsomers2910032
Maprs2910032
PheGenIrs2910032
hapmaprs2910032
1000 genomesrs2910032
hgdprs2910032
ensemblrs2910032
gopubmedrs2910032
geneviewrs2910032
scholarrs2910032
googlers2910032
pharmgkbrs2910032
gwascentralrs2910032
openSNPrs2910032
23andMers2910032
23andMe allrs2910032
SNP Nexus

SNPshotrs2910032
SNPdbers2910032
MSV3drs2910032
GWAS Ctlgrs2910032
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 23974872OA-icon.png]
Trait Schizophrenia
Title Genome-wide association analysis identifies 13 new risk loci for schizophrenia.
Risk Allele C
P-val 4E-8
Odds Ratio 1.08 [1.05-1.11]