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rs9918508

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs9918508(C;T)
Make rs9918508(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position9499649
is asnp
is mentioned by
dbSNPrs9918508
ebirs9918508
HLIrs9918508
Exacrs9918508
Varsomers9918508
Maprs9918508
PheGenIrs9918508
hapmaprs9918508
1000 genomesrs9918508
hgdprs9918508
ensemblrs9918508
gopubmedrs9918508
geneviewrs9918508
scholarrs9918508
googlers9918508
pharmgkbrs9918508
gwascentralrs9918508
openSNPrs9918508
23andMers9918508
23andMe allrs9918508
SNP Nexus

SNPshotrs9918508
SNPdbers9918508
MSV3drs9918508
GWAS Ctlgrs9918508
GMAF0.07025
Max Magnitude0
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 19668339OA-icon.png]
Trait Hippocampal atrophy
Title Hippocampal atrophy as a quantitative trait in a genome-wide association study identifying novel susceptibility genes for Alzheimer's disease
Risk Allele
P-val 0.000008
Odds Ratio NR NR


GET Evidence
rs9918508
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.0625
summary