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rs2074955

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in complete genomics
Make rs2074955(C;C)
Make rs2074955(C;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position158121282
GeneUPP2
is asnp
is mentioned by
dbSNPrs2074955
ebirs2074955
HLIrs2074955
Exacrs2074955
Varsomers2074955
Maprs2074955
PheGenIrs2074955
hapmaprs2074955
1000 genomesrs2074955
hgdprs2074955
ensemblrs2074955
gopubmedrs2074955
geneviewrs2074955
scholarrs2074955
googlers2074955
pharmgkbrs2074955
gwascentralrs2074955
openSNPrs2074955
23andMers2074955
23andMe allrs2074955
SNP Nexus

SNPshotrs2074955
SNPdbers2074955
MSV3drs2074955
GWAS Ctlgrs2074955
GMAF0.1997
Max Magnitude0
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 20932310OA-icon.png]
Trait
Title Genome-wide association reveals genetic effects on human Abeta42 and tau protein levels in cerebrospinal fluids: a case control study
Risk Allele C
P-val 1E-7
Odds Ratio None None