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rs9390537

From SNPedia

Orientationplus
Stabilizedplus
Make rs9390537(C;C)
Make rs9390537(C;T)
Make rs9390537(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position148102235
is asnp
is mentioned by
dbSNPrs9390537
dbSNP (classic)rs9390537
ClinGenrs9390537
ebirs9390537
HLIrs9390537
Exacrs9390537
Gnomadrs9390537
Varsomers9390537
LitVarrs9390537
Maprs9390537
PheGenIrs9390537
Biobankrs9390537
1000 genomesrs9390537
hgdprs9390537
ensemblrs9390537
geneviewrs9390537
scholarrs9390537
googlers9390537
pharmgkbrs9390537
gwascentralrs9390537
openSNPrs9390537
23andMers9390537
SNPshotrs9390537
SNPdbers9390537
MSV3drs9390537
GWAS Ctlgrs9390537
GMAF0.3774
Max Magnitude0
? (C;C) (C;T) (T;T) 28


GWAS snp
PMID [PMID 19749422]
Trait Alzheimer's Disease
Title Genome-Wide Scan of Copy Number Variation in Late-Onset Alzheimer's Disease
Risk Allele
P-val 0.000008
Odds Ratio NR NR
GWAS snp
PMID [PMID 20061627OA-icon.png]
Trait Alzheimer's disease
Title Genome-wide scan of copy number variation in late-onset Alzheimer's disease.
Risk Allele
P-val 0.000008
Odds Ratio None None