Have questions? Visit https://www.reddit.com/r/SNPedia

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
ebirs9390537
HLIrs9390537
Exacrs9390537
Varsomers9390537
Maprs9390537
PheGenIrs9390537
hapmaprs9390537
1000 genomesrs9390537
hgdprs9390537
ensemblrs9390537
gopubmedrs9390537
geneviewrs9390537
scholarrs9390537
googlers9390537
pharmgkbrs9390537
gwascentralrs9390537
openSNPrs9390537
23andMers9390537
23andMe allrs9390537
SNP Nexus

SNPshotrs9390537
SNPdbers9390537
MSV3drs9390537
GWAS Ctlgrs9390537
GMAF0.3774
Max Magnitude
? (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


GET Evidence
rs9390537
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.732759
summary