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rs1920592

From SNPedia

Orientationminus
Stabilizedminus
Make rs1920592(A;A)
Make rs1920592(A;G)
Make rs1920592(G;G)
ReferenceGRCh38 38.1/141
Chromosome12
Position114267781
is asnp
is mentioned by
dbSNPrs1920592
ebirs1920592
HLIrs1920592
Exacrs1920592
Varsomers1920592
Maprs1920592
PheGenIrs1920592
hapmaprs1920592
1000 genomesrs1920592
hgdprs1920592
ensemblrs1920592
gopubmedrs1920592
geneviewrs1920592
scholarrs1920592
googlers1920592
pharmgkbrs1920592
gwascentralrs1920592
openSNPrs1920592
23andMers1920592
23andMe allrs1920592
SNP Nexus

SNPshotrs1920592
SNPdbers1920592
MSV3drs1920592
GWAS Ctlgrs1920592
GMAF0.2576
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 23212062OA-icon.png]
Trait Schizophrenia
Title Genome-wide association study of clinical dimensions of schizophrenia: polygenic effect on disorganized symptoms.
Risk Allele
P-val 1E-6
Odds Ratio .11 [NR] unit decrease