{{Rsnum
|rsid=5742915
|Gene=PML
|Chromosome=15
|position=74044292
|Orientation=plus
|GMAF=0.2268
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=PML
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 21.2 | 58.4 | 20.4
| HCB | 0.0 | 1.5 | 98.5
| JPT | 0.0 | 0.9 | 99.1
| YRI | 0.0 | 4.8 | 95.2
| ASW | 1.8 | 19.3 | 78.9
| CHB | 0.0 | 1.5 | 98.5
| CHD | 0.0 | 0.9 | 99.1
| GIH | 9.9 | 46.5 | 43.6
| LWK | 0.0 | 5.5 | 94.5
| MEX | 8.6 | 32.8 | 58.6
| MKK | 0.0 | 9.0 | 91.0
| TSI | 18.6 | 45.1 | 36.3
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=20881960
|Trait=Height
|Title=Hundreds of variants clustered in genomic loci and biological pathways affect human height
|RiskAllele=T
|Pval=5E-7
|OR=0.03
|ORtxt=[NR] unit decrease
|OA=1
}}

{{PMID Auto GWAS
|PMID=21623375
|Trait=None
|Title=Genome-wide association identifies three new susceptibility loci for Paget's disease of bone.
|RiskAllele=C
|Pval=2E-14
|OR=1.3400
|ORtxt=[1.25-1.45]
}}

{{GET Evidence
|gene=PML
|aa_change=Phe645Leu
|aa_change_short=F645L
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs5742915
|overall_frequency_n=3632
|overall_frequency_d=10758
|overall_frequency=0.337609
|n_genomes=23
|n_genomes_annotated=0
|n_haplomes=31
|n_articles=0
|n_articles_annotated=0
|nblosum100=0
|autoscore=0
|webscore=N
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}