Have questions? Visit https://www.reddit.com/r/SNPedia

rs2054399

From SNPedia

Orientationminus
Stabilizedplus
Make rs2054399(C;C)
Make rs2054399(C;T)
Make rs2054399(T;T)
ReferenceGRCh38 38.1/142
Chromosome3
Position178623794
GeneKCNMB2
is asnp
is mentioned by
dbSNPrs2054399
ebirs2054399
HLIrs2054399
Exacrs2054399
Varsomers2054399
Maprs2054399
PheGenIrs2054399
hapmaprs2054399
1000 genomesrs2054399
hgdprs2054399
ensemblrs2054399
gopubmedrs2054399
geneviewrs2054399
scholarrs2054399
googlers2054399
pharmgkbrs2054399
gwascentralrs2054399
openSNPrs2054399
23andMers2054399
23andMe allrs2054399
SNP Nexus

SNPshotrs2054399
SNPdbers2054399
MSV3drs2054399
GWAS Ctlgrs2054399
GMAF0.3421
Max Magnitude
? (C;C) (C;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 0.000001
Odds Ratio 1.2200 None