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rs1082714

From SNPedia

Orientationplus
Stabilizedplus
Make rs1082714(C;C)
Make rs1082714(C;T)
Make rs1082714(T;T)
ReferenceGRCh38 38.1/141
Chromosome12
Position67235051
is asnp
is mentioned by
dbSNPrs1082714
ebirs1082714
HLIrs1082714
Exacrs1082714
Varsomers1082714
Maprs1082714
PheGenIrs1082714
hapmaprs1082714
1000 genomesrs1082714
hgdprs1082714
ensemblrs1082714
gopubmedrs1082714
geneviewrs1082714
scholarrs1082714
googlers1082714
pharmgkbrs1082714
gwascentralrs1082714
openSNPrs1082714
23andMers1082714
23andMe allrs1082714
SNP Nexus

SNPshotrs1082714
SNPdbers1082714
MSV3drs1082714
GWAS Ctlgrs1082714
GMAF0.4702
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 0.000005
Odds Ratio NR NR


GET Evidence
rs1082714
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.459677
summary