rs4262150
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs4262150(G;G) |
Make rs4262150(G;T) |
Make rs4262150(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 5 |
Position | 152908893 |
Gene | LINC01470 |
is a | snp |
is | mentioned by |
dbSNP | rs4262150 |
dbSNP (classic) | rs4262150 |
ClinGen | rs4262150 |
ebi | rs4262150 |
HLI | rs4262150 |
Exac | rs4262150 |
Gnomad | rs4262150 |
Varsome | rs4262150 |
LitVar | rs4262150 |
Map | rs4262150 |
PheGenI | rs4262150 |
Biobank | rs4262150 |
1000 genomes | rs4262150 |
hgdp | rs4262150 |
ensembl | rs4262150 |
geneview | rs4262150 |
scholar | rs4262150 |
rs4262150 | |
pharmgkb | rs4262150 |
gwascentral | rs4262150 |
openSNP | rs4262150 |
23andMe | rs4262150 |
SNPshot | rs4262150 |
SNPdbe | rs4262150 |
MSV3d | rs4262150 |
GWAS Ctlg | rs4262150 |
GMAF | 0.3154 |
Max Magnitude | 0 |
? | (G;G) (G;T) (T;T) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 22688191![]() |
Trait | |
Title | Genome-wide association study in a Swedish population yields support for greater CNV and MHC involvement in schizophrenia compared with bipolar disorder. |
Risk Allele | |
P-val | 0.000007 |
Odds Ratio | 1.2200 None |