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rs1198588

From SNPedia

Orientationminus
Stabilizedplus
Make rs1198588(A;A)
Make rs1198588(A;T)
Make rs1198588(T;T)
ReferenceGRCh38 38.1/142
Chromosome1
Position98087276
is asnp
is mentioned by
dbSNPrs1198588
ebirs1198588
HLIrs1198588
Exacrs1198588
Varsomers1198588
Maprs1198588
PheGenIrs1198588
hapmaprs1198588
1000 genomesrs1198588
hgdprs1198588
ensemblrs1198588
gopubmedrs1198588
geneviewrs1198588
scholarrs1198588
googlers1198588
pharmgkbrs1198588
gwascentralrs1198588
openSNPrs1198588
23andMers1198588
23andMe allrs1198588
SNP Nexus

SNPshotrs1198588
SNPdbers1198588
MSV3drs1198588
GWAS Ctlgrs1198588
GMAF0.1814
Max Magnitude
? (A;A) (A;T) (T;T) 28
GWAS snp
PMID [PMID 22688191OA-icon.png]
Trait
Title Genome-wide association study in a Swedish population yields support for greater CNV and MHC involvement in schizophrenia compared with bipolar disorder.
Risk Allele
P-val 5E-7
Odds Ratio 1.1200 None
GWAS snp
PMID [PMID 23974872OA-icon.png]
Trait Schizophrenia
Title Genome-wide association analysis identifies 13 new risk loci for schizophrenia.
Risk Allele T
P-val 2E-12
Odds Ratio 1.12 [1.09-1.16]