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rs1768208

From SNPedia

Orientationplus
Stabilizedplus
Make rs1768208(C;C)
Make rs1768208(C;T)
Make rs1768208(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position39481512
GeneMOBP
is asnp
is mentioned by
dbSNPrs1768208
ebirs1768208
HLIrs1768208
Exacrs1768208
Varsomers1768208
Maprs1768208
PheGenIrs1768208
hapmaprs1768208
1000 genomesrs1768208
hgdprs1768208
ensemblrs1768208
gopubmedrs1768208
geneviewrs1768208
scholarrs1768208
googlers1768208
pharmgkbrs1768208
gwascentralrs1768208
openSNPrs1768208
23andMers1768208
23andMe allrs1768208
SNP Nexus

SNPshotrs1768208
SNPdbers1768208
MSV3drs1768208
GWAS Ctlgrs1768208
GMAF0.3489
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 21685912OA-icon.png]
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.