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rs10781380

From SNPedia

Orientationplus
Stabilizedplus
Make rs10781380(C;C)
Make rs10781380(C;T)
Make rs10781380(T;T)
ReferenceGRCh38 38.1/141
Chromosome9
Position76793228
GenePRUNE2
is asnp
is mentioned by
dbSNPrs10781380
ebirs10781380
HLIrs10781380
Exacrs10781380
Varsomers10781380
Maprs10781380
PheGenIrs10781380
hapmaprs10781380
1000 genomesrs10781380
hgdprs10781380
ensemblrs10781380
gopubmedrs10781380
geneviewrs10781380
scholarrs10781380
googlers10781380
pharmgkbrs10781380
gwascentralrs10781380
openSNPrs10781380
23andMers10781380
23andMe allrs10781380
SNP Nexus

SNPshotrs10781380
SNPdbers10781380
MSV3drs10781380
GWAS Ctlgrs10781380
GMAF0.3269
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 7E-7
Odds Ratio NR NR


GET Evidence
rs10781380
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.34375
summary