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rs526904

From SNPedia

Orientationplus
Stabilizedplus
Make rs526904(C;C)
Make rs526904(C;T)
Make rs526904(T;T)
ReferenceGRCh38.p7 38.3/149
Chromosome11
Position86100322
is asnp
is mentioned by
dbSNPrs526904
dbSNP (classic)rs526904
ClinGenrs526904
ebirs526904
HLIrs526904
Exacrs526904
Gnomadrs526904
Varsomers526904
LitVarrs526904
Maprs526904
PheGenIrs526904
Biobankrs526904
1000 genomesrs526904
hgdprs526904
ensemblrs526904
geneviewrs526904
scholarrs526904
googlers526904
pharmgkbrs526904
gwascentralrs526904
openSNPrs526904
23andMers526904
SNPshotrs526904
SNPdbers526904
MSV3drs526904
GWAS Ctlgrs526904
Max Magnitude0
? (C;C) (C;T) (T;T) 28


[PMID 28323831OA-icon.png] Alzheimer's disease polygenic hazard score