rs12666575
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs12666575(C;C) |
Make rs12666575(C;T) |
Make rs12666575(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 7 |
Position | 1964786 |
Gene | MAD1L1 |
is a | snp |
is | mentioned by |
dbSNP | rs12666575 |
dbSNP (classic) | rs12666575 |
ClinGen | rs12666575 |
ebi | rs12666575 |
HLI | rs12666575 |
Exac | rs12666575 |
Gnomad | rs12666575 |
Varsome | rs12666575 |
LitVar | rs12666575 |
Map | rs12666575 |
PheGenI | rs12666575 |
Biobank | rs12666575 |
1000 genomes | rs12666575 |
hgdp | rs12666575 |
ensembl | rs12666575 |
geneview | rs12666575 |
scholar | rs12666575 |
rs12666575 | |
pharmgkb | rs12666575 |
gwascentral | rs12666575 |
openSNP | rs12666575 |
23andMe | rs12666575 |
SNPshot | rs12666575 |
SNPdbe | rs12666575 |
MSV3d | rs12666575 |
GWAS Ctlg | rs12666575 |
GMAF | 0.3264 |
Max Magnitude | 0 |
? | (C;C) (C;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 | 2E-9 |
Odds Ratio | 1.1200 None |