PML, promyelocytic leukemia, 5371

N. diseases: 274; N. variants: 14
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs3784556
rs3784556
Entrez Id: 5371
Gene Symbol: PML
PML
CUI: C0206368
Disease:
Exfoliation Syndrome 		C 0.700 GeneticVariation GWASDB Novel common variants and susceptible haplotype for exfoliation glaucoma specific to Asian population. 24938310 2014
dbSNP: rs3825941
rs3825941
Entrez Id: 5371
Gene Symbol: PML
PML
CUI: C0206368
Disease:
Exfoliation Syndrome 		T 0.700 GeneticVariation GWASDB Novel common variants and susceptible haplotype for exfoliation glaucoma specific to Asian population. 24938310 2014
dbSNP: rs5742915
rs5742915
Entrez Id: 5371
Gene Symbol: PML
PML
CUI: C0005890
Disease:
Body Height 		T 0.700 GeneticVariation GWASCAT Defining the role of common variation in the genomic and biological architecture of adult human height. 25282103 2014
dbSNP: rs8039584
rs8039584
Entrez Id: 5371
Gene Symbol: PML
PML
CUI: C0154778
Disease:
Myopia, Degenerative 		0.700 GeneticVariation GWASCAT A genome-wide association study provides evidence for association of chromosome 8p23 (MYP10) and 10q21.1 (MYP15) with high myopia in the French Population. 23049088 2012
dbSNP: rs3784562
rs3784562
Entrez Id: 5371
Gene Symbol: PML
PML
CUI: C0027051
Disease:
Myocardial Infarction 		0.700 GeneticVariation GWASDB Association of a polymorphism of BTN2A1 with myocardial infarction in East Asian populations. 21211798 2011
dbSNP: rs5742915
rs5742915
Entrez Id: 5371
Gene Symbol: PML
PML
CUI: C1368019
Disease:
Paget Disease 		C 0.700 GeneticVariation GWASDB Genome-wide association identifies three new susceptibility loci for Paget's disease of bone. 21623375 2011
dbSNP: rs5742915
rs5742915
Entrez Id: 5371
Gene Symbol: PML
PML
CUI: C0005890
Disease:
Body Height 		T 0.700 GeneticVariation GWASCAT Hundreds of variants clustered in genomic loci and biological pathways affect human height. 20881960 2010
dbSNP: rs5742915
rs5742915
Entrez Id: 5371
Gene Symbol: PML
PML
CUI: C0489786
Disease:
Height 		T 0.700 GeneticVariation GWASDB Hundreds of variants clustered in genomic loci and biological pathways affect human height. 20881960 2010
dbSNP: rs5742915
rs5742915
Entrez Id: 5371
Gene Symbol: PML
PML
CUI: C0029401
Disease:
Osteitis Deformans 		C 0.800 GeneticVariation GWASCAT Genome-wide association identifies three new susceptibility loci for Paget's disease of bone. 21623375 2011
dbSNP: rs5742915
rs5742915
Entrez Id: 5371
Gene Symbol: PML
PML
CUI: C0029401
Disease:
Osteitis Deformans 		C 0.800 GeneticVariation GWASDB Genome-wide association identifies three new susceptibility loci for Paget's disease of bone. 21623375 2011