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rs7539409

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common on affy axiom data
Make rs7539409(A;G)
Make rs7539409(G;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position83789052
GeneRP11-475O6.1
is asnp
is mentioned by
dbSNPrs7539409
ebirs7539409
HLIrs7539409
Exacrs7539409
Varsomers7539409
Maprs7539409
PheGenIrs7539409
hapmaprs7539409
1000 genomesrs7539409
hgdprs7539409
ensemblrs7539409
gopubmedrs7539409
geneviewrs7539409
scholarrs7539409
googlers7539409
pharmgkbrs7539409
gwascentralrs7539409
openSNPrs7539409
23andMers7539409
23andMe allrs7539409
SNP Nexus

SNPshotrs7539409
SNPdbers7539409
MSV3drs7539409
GWAS Ctlgrs7539409
GMAF0.08173
Max Magnitude0
? (A;A) (A;G) (G;G) 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 0.000001
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 0.000001
Odds Ratio None None


GET Evidence
rs7539409
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.90625
summary