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rs2075713

From SNPedia

Orientationminus
Stabilizedminus
Make rs2075713(G;G)
Make rs2075713(G;T)
Make rs2075713(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position124748043
GeneVSIG2
is asnp
is mentioned by
dbSNPrs2075713
ebirs2075713
HLIrs2075713
Exacrs2075713
Varsomers2075713
Maprs2075713
PheGenIrs2075713
hapmaprs2075713
1000 genomesrs2075713
hgdprs2075713
ensemblrs2075713
gopubmedrs2075713
geneviewrs2075713
scholarrs2075713
googlers2075713
pharmgkbrs2075713
gwascentralrs2075713
openSNPrs2075713
23andMers2075713
23andMe allrs2075713
SNP Nexus

SNPshotrs2075713
SNPdbers2075713
MSV3drs2075713
GWAS Ctlgrs2075713
GMAF0.1942
Max Magnitude
? (G;G) (G;T) (T;T) 28

[PMID 22461181] Functional genetic variation at the NRGN gene and schizophrenia: Evidence from a gene-based case-control study and gene expression analysis