rs1768208
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs1768208(C;C) |
Make rs1768208(C;T) |
Make rs1768208(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 3 |
Position | 39481512 |
Gene | MOBP |
is a | snp |
is | mentioned by |
dbSNP | rs1768208 |
dbSNP (classic) | rs1768208 |
ClinGen | rs1768208 |
ebi | rs1768208 |
HLI | rs1768208 |
Exac | rs1768208 |
Gnomad | rs1768208 |
Varsome | rs1768208 |
LitVar | rs1768208 |
Map | rs1768208 |
PheGenI | rs1768208 |
Biobank | rs1768208 |
1000 genomes | rs1768208 |
hgdp | rs1768208 |
ensembl | rs1768208 |
geneview | rs1768208 |
scholar | rs1768208 |
rs1768208 | |
pharmgkb | rs1768208 |
gwascentral | rs1768208 |
openSNP | rs1768208 |
23andMe | rs1768208 |
SNPshot | rs1768208 |
SNPdbe | rs1768208 |
MSV3d | rs1768208 |
GWAS Ctlg | rs1768208 |
GMAF | 0.3489 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 21685912] |
Trait | |
Title | Identification of common variants influencing risk of the tauopathy progressive supranuclear palsy. |
Risk Allele | |
P-val | 5E-17 |
Odds Ratio | 1.3700 [1.28-1.49] |
[PMID 23116876] An exploratory study on STX6, MOBP, MAPT, and EIF2AK3 and late-onset Alzheimer's disease.
[PMID 26335643] Appoptosin-Mediated Caspase Cleavage of Tau Contributes to Progressive Supranuclear Palsy Pathogenesis
[PMID 27115769] Gene expression, methylation and neuropathology correlations at progressive supranuclear palsy risk loci.