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rs4509693

From SNPedia

Orientationplus
Stabilizedplus
Make rs4509693(C;C)
Make rs4509693(C;T)
Make rs4509693(T;T)
ReferenceGRCh38 38.1/142
Chromosome10
Position100741814
is asnp
is mentioned by
dbSNPrs4509693
ebirs4509693
HLIrs4509693
Exacrs4509693
Varsomers4509693
Maprs4509693
PheGenIrs4509693
hapmaprs4509693
1000 genomesrs4509693
hgdprs4509693
ensemblrs4509693
gopubmedrs4509693
geneviewrs4509693
scholarrs4509693
googlers4509693
pharmgkbrs4509693
gwascentralrs4509693
openSNPrs4509693
23andMers4509693
23andMe allrs4509693
SNP Nexus

SNPshotrs4509693
SNPdbers4509693
MSV3drs4509693
GWAS Ctlgrs4509693
GMAF0.1708
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 0.000006
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 0.000006
Odds Ratio None None


GET Evidence
rs4509693
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.8125
summary