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rs1484642

From SNPedia

Orientationplus
Stabilizedplus
Make rs1484642(C;C)
Make rs1484642(C;G)
Make rs1484642(G;G)
ReferenceGRCh38 38.1/141
Chromosome8
Position10129145
GeneMSRA
is asnp
is mentioned by
dbSNPrs1484642
ebirs1484642
HLIrs1484642
Exacrs1484642
Varsomers1484642
Maprs1484642
PheGenIrs1484642
hapmaprs1484642
1000 genomesrs1484642
hgdprs1484642
ensemblrs1484642
gopubmedrs1484642
geneviewrs1484642
scholarrs1484642
googlers1484642
pharmgkbrs1484642
gwascentralrs1484642
openSNPrs1484642
23andMers1484642
23andMe allrs1484642
SNP Nexus

SNPshotrs1484642
SNPdbers1484642
MSV3drs1484642
GWAS Ctlgrs1484642
GMAF0.07438
Max Magnitude
? (C;C) (C;G) (G;G) 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 C
P-val 0.000003
Odds Ratio 1.4300 None