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rs12071951

From SNPedia

Orientationplus
Stabilizedplus
Make rs12071951(G;G)
Make rs12071951(G;T)
Make rs12071951(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position96648359
is asnp
is mentioned by
dbSNPrs12071951
ebirs12071951
HLIrs12071951
Exacrs12071951
Varsomers12071951
Maprs12071951
PheGenIrs12071951
hapmaprs12071951
1000 genomesrs12071951
hgdprs12071951
ensemblrs12071951
gopubmedrs12071951
geneviewrs12071951
scholarrs12071951
googlers12071951
pharmgkbrs12071951
gwascentralrs12071951
openSNPrs12071951
23andMers12071951
23andMe allrs12071951
SNP Nexus

SNPshotrs12071951
SNPdbers12071951
MSV3drs12071951
GWAS Ctlgrs12071951
GMAF0.2805
Max Magnitude
? (G;G) (G;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 1.1400 None