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rs9877502

From SNPedia

Orientationplus
Stabilizedplus
Make rs9877502(A;A)
Make rs9877502(A;G)
Make rs9877502(G;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position190951729
is asnp
is mentioned by
dbSNPrs9877502
dbSNP (classic)rs9877502
ClinGenrs9877502
ebirs9877502
HLIrs9877502
Exacrs9877502
Gnomadrs9877502
Varsomers9877502
LitVarrs9877502
Maprs9877502
PheGenIrs9877502
Biobankrs9877502
1000 genomesrs9877502
hgdprs9877502
ensemblrs9877502
geneviewrs9877502
scholarrs9877502
googlers9877502
pharmgkbrs9877502
gwascentralrs9877502
openSNPrs9877502
23andMers9877502
SNPshotrs9877502
SNPdbers9877502
MSV3drs9877502
GWAS Ctlgrs9877502
GMAF0.4027
Max Magnitude0
? (A;A) (A;G) (G;G) 28


Linked to increased risk of Alzheimer's disease. [1]

GWAS snp
PMID [PMID 23562540OA-icon.png]
Trait Alzheimer's disease biomarkers
Title GWAS of cerebrospinal fluid tau levels identifies risk variants for Alzheimer's disease.
Risk Allele A
P-val 5E-9
Odds Ratio .05 [NR] unit increase


[PMID 30792413OA-icon.png] Association of IL1RAP-related genetic variation with cerebrospinal fluid concentration of Alzheimer-associated tau protein.