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rs1411478

From SNPedia

Orientationplus
Stabilizedplus
Make rs1411478(A;A)
Make rs1411478(A;G)
Make rs1411478(G;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position180993146
GeneSTX6
is asnp
is mentioned by
dbSNPrs1411478
ebirs1411478
HLIrs1411478
Exacrs1411478
Varsomers1411478
Maprs1411478
PheGenIrs1411478
hapmaprs1411478
1000 genomesrs1411478
hgdprs1411478
ensemblrs1411478
gopubmedrs1411478
geneviewrs1411478
scholarrs1411478
googlers1411478
pharmgkbrs1411478
gwascentralrs1411478
openSNPrs1411478
23andMers1411478
23andMe allrs1411478
SNP Nexus

SNPshotrs1411478
SNPdbers1411478
MSV3drs1411478
GWAS Ctlgrs1411478
GMAF0.4256
Max Magnitude
? (A;A) (A;G) (G;G) 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 4E-11
Odds Ratio 1.2700 [1.19-1.37]


[PMID 23415606] STX6 rs1411478 is not associated with increased risk of Parkinson's disease


[PMID 23116876] An exploratory study on STX6, MOBP, MAPT, and EIF2AK3 and late-onset Alzheimer's disease.