{{Rsnum
|rsid=951660
|Gene=PHLDB2
|Chromosome=3
|position=111919285
|Orientation=plus
|GMAF=0.1249
|Gene_s=PHLDB2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;C)
| geno3=(C;C)
| CEU | 0.0 | 18.6 | 81.4
| HCB | 0.7 | 22.6 | 76.6
| JPT | 0.0 | 4.4 | 95.6
| YRI | 4.1 | 36.7 | 59.2
| ASW | 1.8 | 28.6 | 69.6
| CHB | 0.7 | 22.6 | 76.6
| CHD | 0.9 | 20.2 | 78.9
| GIH | 6.0 | 45.0 | 49.0
| LWK | 5.5 | 41.8 | 52.7
| MEX | 1.7 | 17.2 | 81.0
| MKK | 1.3 | 33.1 | 65.6
| TSI | 1.0 | 14.7 | 84.3
| HapMapRevision=28
}}{{PMID Auto
|PMID=22111664
|Title=Functions of intronic nucleotide variants in the gene encoding pleckstrin homology like domain beta 2 (PHLDB2) on susceptibility to vascular dementia
}}

{{on chip | Affy GenomeWide 6}}
{{on chip | Illumina Human 1M}}