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rs6881634

From SNPedia

Orientationplus
Stabilizedplus
Make rs6881634(A;A)
Make rs6881634(A;G)
Make rs6881634(G;G)
ReferenceGRCh38 38.1/141
Chromosome5
Position78335030
is asnp
is mentioned by
dbSNPrs6881634
ebirs6881634
HLIrs6881634
Exacrs6881634
Varsomers6881634
Maprs6881634
PheGenIrs6881634
hapmaprs6881634
1000 genomesrs6881634
hgdprs6881634
ensemblrs6881634
gopubmedrs6881634
geneviewrs6881634
scholarrs6881634
googlers6881634
pharmgkbrs6881634
gwascentralrs6881634
openSNPrs6881634
23andMers6881634
23andMe allrs6881634
SNP Nexus

SNPshotrs6881634
SNPdbers6881634
MSV3drs6881634
GWAS Ctlgrs6881634
GMAF0.3705
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
rs6881634
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.398438
summary