rs11880923
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs11880923(C;C) |
Make rs11880923(C;T) |
Make rs11880923(T;T) |
Reference | GRCh38 38.1/142 |
Chromosome | 19 |
Position | 49618821 |
Gene | PRR12 |
is a | snp |
is | mentioned by |
dbSNP | rs11880923 |
dbSNP (classic) | rs11880923 |
ClinGen | rs11880923 |
ebi | rs11880923 |
HLI | rs11880923 |
Exac | rs11880923 |
Gnomad | rs11880923 |
Varsome | rs11880923 |
LitVar | rs11880923 |
Map | rs11880923 |
PheGenI | rs11880923 |
Biobank | rs11880923 |
1000 genomes | rs11880923 |
hgdp | rs11880923 |
ensembl | rs11880923 |
geneview | rs11880923 |
scholar | rs11880923 |
rs11880923 | |
pharmgkb | rs11880923 |
gwascentral | rs11880923 |
openSNP | rs11880923 |
23andMe | rs11880923 |
SNPshot | rs11880923 |
SNPdbe | rs11880923 |
MSV3d | rs11880923 |
GWAS Ctlg | rs11880923 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 25843157] Common variants of IRF3 conferring risk of schizophrenia