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rs271738

From SNPedia

Orientationplus
Stabilizedplus
Make rs271738(A;A)
Make rs271738(A;G)
Make rs271738(G;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position234527144
is asnp
is mentioned by
dbSNPrs271738
ebirs271738
HLIrs271738
Exacrs271738
Varsomers271738
Maprs271738
PheGenIrs271738
hapmaprs271738
1000 genomesrs271738
hgdprs271738
ensemblrs271738
gopubmedrs271738
geneviewrs271738
scholarrs271738
googlers271738
pharmgkbrs271738
gwascentralrs271738
openSNPrs271738
23andMers271738
23andMe allrs271738
SNP Nexus

SNPshotrs271738
SNPdbers271738
MSV3drs271738
GWAS Ctlgrs271738
GMAF0.3586
Max Magnitude
? (A;A) (A;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 A
P-val 0.000005
Odds Ratio 1.3200 None