rs11210359
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs11210359(A;A) |
Make rs11210359(A;G) |
Make rs11210359(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 1 |
Position | 73873484 |
is a | snp |
is | mentioned by |
dbSNP | rs11210359 |
dbSNP (classic) | rs11210359 |
ClinGen | rs11210359 |
ebi | rs11210359 |
HLI | rs11210359 |
Exac | rs11210359 |
Gnomad | rs11210359 |
Varsome | rs11210359 |
LitVar | rs11210359 |
Map | rs11210359 |
PheGenI | rs11210359 |
Biobank | rs11210359 |
1000 genomes | rs11210359 |
hgdp | rs11210359 |
ensembl | rs11210359 |
geneview | rs11210359 |
scholar | rs11210359 |
rs11210359 | |
pharmgkb | rs11210359 |
gwascentral | rs11210359 |
openSNP | rs11210359 |
23andMe | rs11210359 |
SNPshot | rs11210359 |
SNPdbe | rs11210359 |
MSV3d | rs11210359 |
GWAS Ctlg | rs11210359 |
GMAF | 0.3522 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 21057379] |
Trait | |
Title | Case-case genome-wide association analysis shows markers differentially associated with schizophrenia and bipolar disorder and implicates calcium channel genes |
Risk Allele | |
P-val | 0.000008 |
Odds Ratio | None None |