rs9315702
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs9315702(A;A) |
Make rs9315702(A;C) |
Make rs9315702(C;C) |
Reference | GRCh38 38.1/141 |
Chromosome | 13 |
Position | 39543931 |
Gene | LHFP |
is a | snp |
is | mentioned by |
dbSNP | rs9315702 |
dbSNP (classic) | rs9315702 |
ClinGen | rs9315702 |
ebi | rs9315702 |
HLI | rs9315702 |
Exac | rs9315702 |
Gnomad | rs9315702 |
Varsome | rs9315702 |
LitVar | rs9315702 |
Map | rs9315702 |
PheGenI | rs9315702 |
Biobank | rs9315702 |
1000 genomes | rs9315702 |
hgdp | rs9315702 |
ensembl | rs9315702 |
geneview | rs9315702 |
scholar | rs9315702 |
rs9315702 | |
pharmgkb | rs9315702 |
gwascentral | rs9315702 |
openSNP | rs9315702 |
23andMe | rs9315702 |
SNPshot | rs9315702 |
SNPdbe | rs9315702 |
MSV3d | rs9315702 |
GWAS Ctlg | rs9315702 |
GMAF | 0.286 |
Max Magnitude | 0 |
? | (A;A) (A;C) (C;C) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 22745009] |
Trait | |
Title | Multiple loci influencing hippocampal degeneration identified by genome scan. |
Risk Allele | A |
P-val | 2E-8 |
Odds Ratio | None None |