rs7192086
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs7192086(A;A) |
Make rs7192086(A;T) |
Make rs7192086(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 16 |
Position | 12967754 |
Gene | SHISA9 |
is a | snp |
is | mentioned by |
dbSNP | rs7192086 |
dbSNP (classic) | rs7192086 |
ClinGen | rs7192086 |
ebi | rs7192086 |
HLI | rs7192086 |
Exac | rs7192086 |
Gnomad | rs7192086 |
Varsome | rs7192086 |
LitVar | rs7192086 |
Map | rs7192086 |
PheGenI | rs7192086 |
Biobank | rs7192086 |
1000 genomes | rs7192086 |
hgdp | rs7192086 |
ensembl | rs7192086 |
geneview | rs7192086 |
scholar | rs7192086 |
rs7192086 | |
pharmgkb | rs7192086 |
gwascentral | rs7192086 |
openSNP | rs7192086 |
23andMe | rs7192086 |
SNPshot | rs7192086 |
SNPdbe | rs7192086 |
MSV3d | rs7192086 |
GWAS Ctlg | rs7192086 |
GMAF | 0.2241 |
Max Magnitude | 0 |
? | (A;A) (A;T) (T;T) | 28 |
---|---|---|
|
GWAS | |
---|---|
SNP | rs7192086 |
PubMedID | [PMID 18677311] |
Condition | Schizophrenia |
Gene | Intergenic |
Risk Allele | T |
pValue | 6.00E-006 |
OR | 1.12 |
95% CI |
[PMID 19396477] A novel 16p locus associated with BSCL2 hereditary motor neuronopathy: a genetic modifier?
[PMID 22005930] Genome-wide association study of Alzheimer's disease with psychotic symptoms.