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rs10494326

From SNPedia

Orientationplus
Stabilizedplus
Make rs10494326(C;C)
Make rs10494326(C;T)
Make rs10494326(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position159679910
is asnp
is mentioned by
dbSNPrs10494326
ebirs10494326
HLIrs10494326
Exacrs10494326
Varsomers10494326
Maprs10494326
PheGenIrs10494326
hapmaprs10494326
1000 genomesrs10494326
hgdprs10494326
ensemblrs10494326
gopubmedrs10494326
geneviewrs10494326
scholarrs10494326
googlers10494326
pharmgkbrs10494326
gwascentralrs10494326
openSNPrs10494326
23andMers10494326
23andMe allrs10494326
SNP Nexus

SNPshotrs10494326
SNPdbers10494326
MSV3drs10494326
GWAS Ctlgrs10494326
Merged fromRs16827466
GMAF0.04178
Max Magnitude
? (C;C) (C;T) (T;T) 28
[PMID 17564960OA-icon.png] A genomewide screen for late-onset Alzheimer disease in a genetically isolated Dutch population.