rs959695
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs959695(A;A) |
Make rs959695(A;G) |
Make rs959695(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 8 |
Position | 99822954 |
Gene | VPS13B |
is a | snp |
is | mentioned by |
dbSNP | rs959695 |
dbSNP (classic) | rs959695 |
ClinGen | rs959695 |
ebi | rs959695 |
HLI | rs959695 |
Exac | rs959695 |
Gnomad | rs959695 |
Varsome | rs959695 |
LitVar | rs959695 |
Map | rs959695 |
PheGenI | rs959695 |
Biobank | rs959695 |
1000 genomes | rs959695 |
hgdp | rs959695 |
ensembl | rs959695 |
geneview | rs959695 |
scholar | rs959695 |
rs959695 | |
pharmgkb | rs959695 |
gwascentral | rs959695 |
openSNP | rs959695 |
23andMe | rs959695 |
SNPshot | rs959695 |
SNPdbe | rs959695 |
MSV3d | rs959695 |
GWAS Ctlg | rs959695 |
GMAF | 0.4137 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 22745009] |
Trait | |
Title | Multiple loci influencing hippocampal degeneration identified by genome scan. |
Risk Allele | C |
P-val | 0.000001 |
Odds Ratio | None None |