rs12278912
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs12278912(A;A) |
Make rs12278912(A;G) |
Make rs12278912(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 11 |
Position | 124742263 |
Gene | NRGN |
is a | snp |
is | mentioned by |
dbSNP | rs12278912 |
dbSNP (classic) | rs12278912 |
ClinGen | rs12278912 |
ebi | rs12278912 |
HLI | rs12278912 |
Exac | rs12278912 |
Gnomad | rs12278912 |
Varsome | rs12278912 |
LitVar | rs12278912 |
Map | rs12278912 |
PheGenI | rs12278912 |
Biobank | rs12278912 |
1000 genomes | rs12278912 |
hgdp | rs12278912 |
ensembl | rs12278912 |
geneview | rs12278912 |
scholar | rs12278912 |
rs12278912 | |
pharmgkb | rs12278912 |
gwascentral | rs12278912 |
openSNP | rs12278912 |
23andMe | rs12278912 |
SNPshot | rs12278912 |
SNPdbe | rs12278912 |
MSV3d | rs12278912 |
GWAS Ctlg | rs12278912 |
GMAF | 0.2902 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 22461181] Functional genetic variation at the NRGN gene and schizophrenia: Evidence from a gene-based case-control study and gene expression analysis