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rs7116190

From SNPedia

Orientationplus
Stabilizedplus
Make rs7116190(A;A)
Make rs7116190(A;G)
Make rs7116190(G;G)
ReferenceGRCh38.p7 38.3/149
Chromosome11
Position60197519
is asnp
is mentioned by
dbSNPrs7116190
dbSNP (classic)rs7116190
ClinGenrs7116190
ebirs7116190
HLIrs7116190
Exacrs7116190
Gnomadrs7116190
Varsomers7116190
LitVarrs7116190
Maprs7116190
PheGenIrs7116190
Biobankrs7116190
1000 genomesrs7116190
hgdprs7116190
ensemblrs7116190
geneviewrs7116190
scholarrs7116190
googlers7116190
pharmgkbrs7116190
gwascentralrs7116190
openSNPrs7116190
23andMers7116190
SNPshotrs7116190
SNPdbers7116190
MSV3drs7116190
GWAS Ctlgrs7116190
Max Magnitude0

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