rs239713
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs239713(C;C) |
Make rs239713(C;T) |
Make rs239713(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 21 |
Position | 27324157 |
Gene | LOC102724355 |
is a | snp |
is | mentioned by |
dbSNP | rs239713 |
dbSNP (classic) | rs239713 |
ClinGen | rs239713 |
ebi | rs239713 |
HLI | rs239713 |
Exac | rs239713 |
Gnomad | rs239713 |
Varsome | rs239713 |
LitVar | rs239713 |
Map | rs239713 |
PheGenI | rs239713 |
Biobank | rs239713 |
1000 genomes | rs239713 |
hgdp | rs239713 |
ensembl | rs239713 |
geneview | rs239713 |
scholar | rs239713 |
rs239713 | |
pharmgkb | rs239713 |
gwascentral | rs239713 |
openSNP | rs239713 |
23andMe | rs239713 |
SNPshot | rs239713 |
SNPdbe | rs239713 |
MSV3d | rs239713 |
GWAS Ctlg | rs239713 |
GMAF | 0.292 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 20932310] |
Trait | |
Title | Genome-wide association reveals genetic effects on human Abeta42 and tau protein levels in cerebrospinal fluids: a case control study |
Risk Allele | T |
P-val | 5E-7 |
Odds Ratio | None None |