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rs2312147

From SNPedia

Orientationplus
Stabilizedplus
Make rs2312147(C;C)
Make rs2312147(C;T)
Make rs2312147(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position57995793
GeneVRK2
is asnp
is mentioned by
dbSNPrs2312147
ebirs2312147
HLIrs2312147
Exacrs2312147
Varsomers2312147
Maprs2312147
PheGenIrs2312147
hapmaprs2312147
1000 genomesrs2312147
hgdprs2312147
ensemblrs2312147
gopubmedrs2312147
geneviewrs2312147
scholarrs2312147
googlers2312147
pharmgkbrs2312147
gwascentralrs2312147
openSNPrs2312147
23andMers2312147
23andMe allrs2312147
SNP Nexus

SNPshotrs2312147
SNPdbers2312147
MSV3drs2312147
GWAS Ctlgrs2312147
GMAF0.2764
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 19571808OA-icon.png]
Trait Schizophrenia
Title Common variants conferring risk of schizophrenia
Risk Allele C
P-val 3E-7
Odds Ratio 1.09 [NR]

[PMID 21791550OA-icon.png] Common variants at VRK2 and TCF4 conferring risk of schizophrenia.


GET Evidence
rs2312147
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.75
summary



[PMID 23102693] Meta-analysis and brain imaging data support the involvement of VRK2 (rs2312147) in schizophrenia susceptibility.


[PMID 27382989] Further evidence of VRK2 rs2312147 associated with schizophrenia.