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rs4530903

From SNPedia

Orientationplus
Stabilizedplus
Make rs4530903(C;C)
Make rs4530903(C;T)
Make rs4530903(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position32614112
is asnp
is mentioned by
dbSNPrs4530903
ebirs4530903
HLIrs4530903
Exacrs4530903
Varsomers4530903
Maprs4530903
PheGenIrs4530903
hapmaprs4530903
1000 genomesrs4530903
hgdprs4530903
ensemblrs4530903
gopubmedrs4530903
geneviewrs4530903
scholarrs4530903
googlers4530903
pharmgkbrs4530903
gwascentralrs4530903
openSNPrs4530903
23andMers4530903
23andMe allrs4530903
SNP Nexus

SNPshotrs4530903
SNPdbers4530903
MSV3drs4530903
GWAS Ctlgrs4530903
GMAF0.08264
Max Magnitude
? (C;C) (C;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 5E-6
Odds Ratio .09 [NR] unit increase
GWAS snp
PMID [PMID 23349640OA-icon.png]
Trait Lymphoma
Title Susceptibility loci associated with specific and shared subtypes of lymphoid malignancies.
Risk Allele T
P-val 3E-12
Odds Ratio 1.93 [NR]