YLPM1, YLP motif containing 1, 56252

N. diseases: 9; N. variants: 8
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2058919
rs2058919
Entrez Id: 56252
Gene Symbol: YLPM1
YLPM1
CUI: C0427460
Disease:
Red cell distribution width determination 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs2058919
rs2058919
Entrez Id: 56252
Gene Symbol: YLPM1
YLPM1
CUI: C1304746
Disease:
RDW - Red blood cell distribution width result 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs10144845
rs10144845
Entrez Id: 56252
Gene Symbol: YLPM1
YLPM1
CUI: C0525045
Disease:
Mood Disorders 		C 0.700 GeneticVariation GWASCAT Meta-analysis of genome-wide association studies for neuroticism in 449,484 individuals identifies novel genetic loci and pathways. 29942085 2018
dbSNP: rs10144845
rs10144845
Entrez Id: 56252
Gene Symbol: YLPM1
YLPM1
CUI: C1269683
Disease:
Major Depressive Disorder 		C 0.700 GeneticVariation GWASCAT Meta-analysis of genome-wide association studies for neuroticism in 449,484 individuals identifies novel genetic loci and pathways. 29942085 2018
dbSNP: rs10148293
rs10148293
Entrez Id: 56252
Gene Symbol: YLPM1
YLPM1
CUI: C1269683
Disease:
Major Depressive Disorder 		G 0.700 GeneticVariation GWASCAT Genome-wide association study of depression phenotypes in UK Biobank identifies variants in excitatory synaptic pathways. 29662059 2018
dbSNP: rs12588415
rs12588415
Entrez Id: 56252
Gene Symbol: YLPM1
YLPM1
CUI: C1445957
Disease:
Serum total cholesterol measurement 		G 0.700 GeneticVariation GWASCAT A large electronic-health-record-based genome-wide study of serum lipids. 29507422 2018
dbSNP: rs2193596
rs2193596
Entrez Id: 56252
Gene Symbol: YLPM1
YLPM1
CUI: C0027769
Disease:
Nervousness 		T 0.700 GeneticVariation GWASCAT Item-level analyses reveal genetic heterogeneity in neuroticism. 29500382 2018
dbSNP: rs2286910
rs2286910
Entrez Id: 56252;283571
Gene Symbol: YLPM1;PROX2
YLPM1;PROX2
CUI: C0023467
Disease:
Leukemia, Myelocytic, Acute 		A 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959 2017
dbSNP: rs8014204
rs8014204
Entrez Id: 56252;283571
Gene Symbol: YLPM1;PROX2
YLPM1;PROX2
CUI: C0023467
Disease:
Leukemia, Myelocytic, Acute 		A 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959 2017
dbSNP: rs8014204
rs8014204
Entrez Id: 56252;283571
Gene Symbol: YLPM1;PROX2
YLPM1;PROX2
CUI: C1445957
Disease:
Serum total cholesterol measurement 		A 0.700 GeneticVariation GWASCAT Exome-wide association study of plasma lipids in >300,000 individuals. 29083408 2017
dbSNP: rs7146395
rs7146395
Entrez Id: 56252
Gene Symbol: YLPM1
YLPM1
CUI: C0032181
Disease:
Platelet Count measurement 		C 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016