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rs690705

From SNPedia

Orientationplus
Stabilizedplus
Make rs690705(A;A)
Make rs690705(A;G)
Make rs690705(G;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position34080781
is asnp
is mentioned by
dbSNPrs690705
ebirs690705
HLIrs690705
Exacrs690705
Varsomers690705
Maprs690705
PheGenIrs690705
hapmaprs690705
1000 genomesrs690705
hgdprs690705
ensemblrs690705
gopubmedrs690705
geneviewrs690705
scholarrs690705
googlers690705
pharmgkbrs690705
gwascentralrs690705
openSNPrs690705
23andMers690705
23andMe allrs690705
SNP Nexus

SNPshotrs690705
SNPdbers690705
MSV3drs690705
GWAS Ctlgrs690705
GMAF0.3251
Max Magnitude
? (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 6E-7
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 6E-7
Odds Ratio None None


GET Evidence
rs690705
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.351562
summary