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rs6031882

From SNPedia

Orientationplus
Stabilizedplus
Make rs6031882(C;C)
Make rs6031882(C;T)
Make rs6031882(T;T)
ReferenceGRCh38 38.1/141
Chromosome20
Position37181380
GeneC20orf132, RPN2
is asnp
is mentioned by
dbSNPrs6031882
ebirs6031882
HLIrs6031882
Exacrs6031882
Varsomers6031882
Maprs6031882
PheGenIrs6031882
hapmaprs6031882
1000 genomesrs6031882
hgdprs6031882
ensemblrs6031882
gopubmedrs6031882
geneviewrs6031882
scholarrs6031882
googlers6031882
pharmgkbrs6031882
gwascentralrs6031882
openSNPrs6031882
23andMers6031882
23andMe allrs6031882
SNP Nexus

SNPshotrs6031882
SNPdbers6031882
MSV3drs6031882
GWAS Ctlgrs6031882
GMAF0.3297
Max Magnitude
? (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 0.000006
Odds Ratio NR NR


GET Evidence
rs6031882
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.414062
summary