rs7872515
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs7872515(A;A) |
Make rs7872515(A;G) |
Make rs7872515(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 9 |
Position | 92060258 |
Gene | SPTLC1 |
is a | snp |
is | mentioned by |
dbSNP | rs7872515 |
dbSNP (classic) | rs7872515 |
ClinGen | rs7872515 |
ebi | rs7872515 |
HLI | rs7872515 |
Exac | rs7872515 |
Gnomad | rs7872515 |
Varsome | rs7872515 |
LitVar | rs7872515 |
Map | rs7872515 |
PheGenI | rs7872515 |
Biobank | rs7872515 |
1000 genomes | rs7872515 |
hgdp | rs7872515 |
ensembl | rs7872515 |
geneview | rs7872515 |
scholar | rs7872515 |
rs7872515 | |
pharmgkb | rs7872515 |
gwascentral | rs7872515 |
openSNP | rs7872515 |
23andMe | rs7872515 |
SNPshot | rs7872515 |
SNPdbe | rs7872515 |
MSV3d | rs7872515 |
GWAS Ctlg | rs7872515 |
GMAF | 0.2971 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 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 | 6E-7 |
Odds Ratio | 1.3900 None |