rs1783925
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs1783925(C;C) |
Make rs1783925(C;T) |
Make rs1783925(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 11 |
Position | 125434113 |
Gene | PKNOX2 |
is a | snp |
is | mentioned by |
dbSNP | rs1783925 |
dbSNP (classic) | rs1783925 |
ClinGen | rs1783925 |
ebi | rs1783925 |
HLI | rs1783925 |
Exac | rs1783925 |
Gnomad | rs1783925 |
Varsome | rs1783925 |
LitVar | rs1783925 |
Map | rs1783925 |
PheGenI | rs1783925 |
Biobank | rs1783925 |
1000 genomes | rs1783925 |
hgdp | rs1783925 |
ensembl | rs1783925 |
geneview | rs1783925 |
scholar | rs1783925 |
rs1783925 | |
pharmgkb | rs1783925 |
gwascentral | rs1783925 |
openSNP | rs1783925 |
23andMe | rs1783925 |
SNPshot | rs1783925 |
SNPdbe | rs1783925 |
MSV3d | rs1783925 |
GWAS Ctlg | rs1783925 |
GMAF | 0.2989 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 22648509] |
Trait | |
Title | PKNOX2 is Associated with Formal Thought Disorder in Schizophrenia: a Meta-Analysis of Two Genome-wide Association Studies. |
Risk Allele | |
P-val | 4E-7 |
Odds Ratio | 1.3900 None |