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rs75617873

From SNPedia

Orientationplus
Stabilizedplus
Make rs75617873(A;A)
Make rs75617873(A;C)
Make rs75617873(C;C)
ReferenceGRCh38 38.1/141
Chromosome22
Position44130225
GenePARVB
is asnp
is mentioned by
dbSNPrs75617873
ebirs75617873
HLIrs75617873
Exacrs75617873
Varsomers75617873
Maprs75617873
PheGenIrs75617873
hapmaprs75617873
1000 genomesrs75617873
hgdprs75617873
ensemblrs75617873
gopubmedrs75617873
geneviewrs75617873
scholarrs75617873
googlers75617873
pharmgkbrs75617873
gwascentralrs75617873
openSNPrs75617873
23andMers75617873
23andMe allrs75617873
SNP Nexus

SNPshotrs75617873
SNPdbers75617873
MSV3drs75617873
GWAS Ctlgrs75617873
GMAF0.01837
Max Magnitude
GWAS snp
PMID [PMID 23535033OA-icon.png]
Trait Alzheimer's disease (cognitive decline)
Title Genome-wide association study of the rate of cognitive decline in Alzheimer's disease.
Risk Allele
P-val 5E-7
Odds Ratio .17 unit decrease