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rs4380187

From SNPedia

Orientationplus
Stabilizedplus
Make rs4380187(A;A)
Make rs4380187(A;C)
Make rs4380187(C;C)
ReferenceGRCh38 38.1/142
Chromosome2
Position184947213
is asnp
is mentioned by
dbSNPrs4380187
dbSNP (classic)rs4380187
ClinGenrs4380187
ebirs4380187
HLIrs4380187
Exacrs4380187
Gnomadrs4380187
Varsomers4380187
LitVarrs4380187
Maprs4380187
PheGenIrs4380187
Biobankrs4380187
1000 genomesrs4380187
hgdprs4380187
ensemblrs4380187
geneviewrs4380187
scholarrs4380187
googlers4380187
pharmgkbrs4380187
gwascentralrs4380187
openSNPrs4380187
23andMers4380187
SNPshotrs4380187
SNPdbers4380187
MSV3drs4380187
GWAS Ctlgrs4380187
Max Magnitude0
? (A;A) (A;C) (C;C) 28


GWAS snp
PMID [PMID 23974872OA-icon.png]
Trait Schizophrenia
Title Genome-wide association analysis identifies 13 new risk loci for schizophrenia.
Risk Allele A
P-val 6E-8
Odds Ratio 1.08 [1.05-1.11]


[PMID 33522046] Evaluation of the relationship between VRK2, rs4380187 polymorphisms, and genetic susceptibility to schizophrenia in the Chinese Han population.