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rs8115854

From SNPedia

Orientationplus
Stabilizedplus
Make rs8115854(A;A)
Make rs8115854(A;G)
Make rs8115854(G;G)
ReferenceGRCh38 38.1/141
Chromosome20
Position37137934
GeneMROH8
is asnp
is mentioned by
dbSNPrs8115854
ebirs8115854
HLIrs8115854
Exacrs8115854
Varsomers8115854
Maprs8115854
PheGenIrs8115854
hapmaprs8115854
1000 genomesrs8115854
hgdprs8115854
ensemblrs8115854
gopubmedrs8115854
geneviewrs8115854
scholarrs8115854
googlers8115854
pharmgkbrs8115854
gwascentralrs8115854
openSNPrs8115854
23andMers8115854
23andMe allrs8115854
SNP Nexus

SNPshotrs8115854
SNPdbers8115854
MSV3drs8115854
GWAS Ctlgrs8115854
GMAF0.3095
Max Magnitude
? (A;A) (A;G) (G;G) 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 0.000002
Odds Ratio NR NR


GET Evidence
C20ORF132-S429P
aa_change Ser429Pro
aa_change_short S429P
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.40625
summary