Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs5758999
rs5758999
Entrez Id: 11252
Gene Symbol: PACSIN2
PACSIN2
CUI: C0005890
Disease:
Body Height
0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs2256040
rs2256040
Entrez Id: 11252
Gene Symbol: PACSIN2
PACSIN2
CUI: C3828530
Disease:
Platelet Component Distribution Width Measurement
A 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs8137128
rs8137128
Entrez Id: 11252
Gene Symbol: PACSIN2
PACSIN2
CUI: C0032181
Disease:
Platelet Count measurement
T 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs972578
rs972578
Entrez Id: 11252
Gene Symbol: PACSIN2
PACSIN2
CUI: C0200665
Disease:
Platelet mean volume determination (procedure)
T 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs7511534
rs7511534
Entrez Id: 11252
Gene Symbol: PACSIN2
PACSIN2
CUI: C0200635
Disease:
Lymphocyte Count measurement
0.700 GeneticVariation GWASDB The combination of a genome-wide association study of lymphocyte count and analysis of gene expression data reveals novel asthma candidate genes. 22286170 2012
dbSNP: rs2413739
rs2413739
Entrez Id: 11252
Gene Symbol: PACSIN2
PACSIN2
CUI: C0751606
Disease:
Adult Acute Lymphocytic Leukemia
0.010 GeneticVariation BEFREE The aim of the study was to validate the impact of the single-nucleotide polymorphism rs2413739 (T > C) in the PACSIN2 gene on thiopurines pharmacological parameters and clinical response in an Italian cohort of pediatric patients with acute lymphoblastic leukemia (ALL) and inflammatory bowel disease (IBD). 31792371 2019
dbSNP: rs2413739
rs2413739
Entrez Id: 11252
Gene Symbol: PACSIN2
PACSIN2
CUI: C0021390
Disease:
Inflammatory Bowel Diseases
0.010 GeneticVariation BEFREE The aim of the study was to validate the impact of the single-nucleotide polymorphism rs2413739 (T > C) in the PACSIN2 gene on thiopurines pharmacological parameters and clinical response in an Italian cohort of pediatric patients with acute lymphoblastic leukemia (ALL) and inflammatory bowel disease (IBD). 31792371 2019
dbSNP: rs2413739
rs2413739
Entrez Id: 11252
Gene Symbol: PACSIN2
PACSIN2
CUI: C0023449
Disease:
Acute lymphocytic leukemia
0.010 GeneticVariation BEFREE The aim of the study was to validate the impact of the single-nucleotide polymorphism rs2413739 (T > C) in the PACSIN2 gene on thiopurines pharmacological parameters and clinical response in an Italian cohort of pediatric patients with acute lymphoblastic leukemia (ALL) and inflammatory bowel disease (IBD). 31792371 2019
dbSNP: rs2413739
rs2413739
Entrez Id: 11252
Gene Symbol: PACSIN2
PACSIN2
CUI: C0023452
Disease:
Childhood Acute Lymphoblastic Leukemia
0.010 GeneticVariation BEFREE The aim of the study was to validate the impact of the single-nucleotide polymorphism rs2413739 (T > C) in the PACSIN2 gene on thiopurines pharmacological parameters and clinical response in an Italian cohort of pediatric patients with acute lymphoblastic leukemia (ALL) and inflammatory bowel disease (IBD). 31792371 2019
dbSNP: rs2413739
rs2413739
Entrez Id: 11252
Gene Symbol: PACSIN2
PACSIN2
CUI: C0023418
Disease:
leukemia
0.010 GeneticVariation BEFREE The association of a PACSIN2 SNP (rs2413739) with TPMT activity was confirmed in patients and knock-down of PACSIN2 mRNA in human leukemia cells (NALM6) resulted in significantly lower TPMT activity. 22846425 2012
dbSNP: rs2413739
rs2413739
Entrez Id: 11252
Gene Symbol: PACSIN2
PACSIN2
CUI: C1332977
Disease:
Childhood Leukemia
0.010 GeneticVariation BEFREE The association of a PACSIN2 SNP (rs2413739) with TPMT activity was confirmed in patients and knock-down of PACSIN2 mRNA in human leukemia cells (NALM6) resulted in significantly lower TPMT activity. 22846425 2012