rs951660
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs951660(A;A) |
Make rs951660(A;C) |
Make rs951660(C;C) |
Reference | GRCh38 38.1/141 |
Chromosome | 3 |
Position | 111919285 |
Gene | PHLDB2 |
is a | snp |
is | mentioned by |
dbSNP | rs951660 |
dbSNP (classic) | rs951660 |
ClinGen | rs951660 |
ebi | rs951660 |
HLI | rs951660 |
Exac | rs951660 |
Gnomad | rs951660 |
Varsome | rs951660 |
LitVar | rs951660 |
Map | rs951660 |
PheGenI | rs951660 |
Biobank | rs951660 |
1000 genomes | rs951660 |
hgdp | rs951660 |
ensembl | rs951660 |
geneview | rs951660 |
scholar | rs951660 |
rs951660 | |
pharmgkb | rs951660 |
gwascentral | rs951660 |
openSNP | rs951660 |
23andMe | rs951660 |
SNPshot | rs951660 |
SNPdbe | rs951660 |
MSV3d | rs951660 |
GWAS Ctlg | rs951660 |
GMAF | 0.1249 |
Max Magnitude | 0 |
? | (A;A) (A;C) (C;C) | 28 |
---|---|---|
|
[PMID 22111664] Functions of intronic nucleotide variants in the gene encoding pleckstrin homology like domain beta 2 (PHLDB2) on susceptibility to vascular dementia