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rs2142991

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common on affy axiom data
Make rs2142991(A;G)
Make rs2142991(G;G)
ReferenceGRCh38 38.1/142
Chromosome10
Position42845657
is asnp
is mentioned by
dbSNPrs2142991
ebirs2142991
HLIrs2142991
Exacrs2142991
Varsomers2142991
Maprs2142991
PheGenIrs2142991
hapmaprs2142991
1000 genomesrs2142991
hgdprs2142991
ensemblrs2142991
gopubmedrs2142991
geneviewrs2142991
scholarrs2142991
googlers2142991
pharmgkbrs2142991
gwascentralrs2142991
openSNPrs2142991
23andMers2142991
23andMe allrs2142991
SNP Nexus

SNPshotrs2142991
SNPdbers2142991
MSV3drs2142991
GWAS Ctlgrs2142991
GMAF0.1414
Max Magnitude0
? (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 3E-7
Odds Ratio 1.3000 [1.18-1.44]