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rs682748

From SNPedia

Orientationminus
Stabilizedminus
Make rs682748(C;C)
Make rs682748(C;T)
Make rs682748(T;T)
ReferenceGRCh38 38.1/142
Chromosome5
Position17148802
GeneCCL14
is asnp
is mentioned by
dbSNPrs682748
ebirs682748
HLIrs682748
Exacrs682748
Varsomers682748
Maprs682748
PheGenIrs682748
hapmaprs682748
1000 genomesrs682748
hgdprs682748
ensemblrs682748
gopubmedrs682748
geneviewrs682748
scholarrs682748
googlers682748
pharmgkbrs682748
gwascentralrs682748
openSNPrs682748
23andMers682748
23andMe allrs682748
SNP Nexus

SNPshotrs682748
SNPdbers682748
MSV3drs682748
GWAS Ctlgrs682748
GMAF0.4858
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 0.000008
Odds Ratio NR NR


GET Evidence
rs682748
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.52381
summary