PMF1, polyamine modulated factor 1, 11243

N. diseases: 11; N. variants: 31
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2758609
rs2758609
Entrez Id: 11243;100527963
Gene Symbol: PMF1;PMF1-BGLAP
PMF1;PMF1-BGLAP
CUI: C2937358
Disease:
Cerebral Hemorrhage
0.700 GeneticVariation GWASDB Meta-analysis of genome-wide association studies identifies 1q22 as a susceptibility locus for intracerebral hemorrhage. 24656865 2014
dbSNP: rs2842870
rs2842870
Entrez Id: 11243;100527963
Gene Symbol: PMF1;PMF1-BGLAP
PMF1;PMF1-BGLAP
CUI: C2937358
Disease:
Cerebral Hemorrhage
0.700 GeneticVariation GWASDB Meta-analysis of genome-wide association studies identifies 1q22 as a susceptibility locus for intracerebral hemorrhage. 24656865 2014
dbSNP: rs2842873
rs2842873
Entrez Id: 11243;100527963
Gene Symbol: PMF1;PMF1-BGLAP
PMF1;PMF1-BGLAP
CUI: C2937358
Disease:
Cerebral Hemorrhage
0.700 GeneticVariation GWASDB Meta-analysis of genome-wide association studies identifies 1q22 as a susceptibility locus for intracerebral hemorrhage. 24656865 2014
dbSNP: rs2853641
rs2853641
Entrez Id: 9673;11243;100527963
Gene Symbol: SLC25A44;PMF1;PMF1-BGLAP
SLC25A44;PMF1;PMF1-BGLAP
CUI: C2937358
Disease:
Cerebral Hemorrhage
0.700 GeneticVariation GWASDB Meta-analysis of genome-wide association studies identifies 1q22 as a susceptibility locus for intracerebral hemorrhage. 24656865 2014
dbSNP: rs2853643
rs2853643
Entrez Id: 11243;100527963
Gene Symbol: PMF1;PMF1-BGLAP
PMF1;PMF1-BGLAP
CUI: C2937358
Disease:
Cerebral Hemorrhage
0.700 GeneticVariation GWASDB Meta-analysis of genome-wide association studies identifies 1q22 as a susceptibility locus for intracerebral hemorrhage. 24656865 2014
dbSNP: rs2853646
rs2853646
Entrez Id: 11243;100527963
Gene Symbol: PMF1;PMF1-BGLAP
PMF1;PMF1-BGLAP
CUI: C2937358
Disease:
Cerebral Hemorrhage
0.700 GeneticVariation GWASDB Meta-analysis of genome-wide association studies identifies 1q22 as a susceptibility locus for intracerebral hemorrhage. 24656865 2014
dbSNP: rs3001789
rs3001789
Entrez Id: 11243;100527963
Gene Symbol: PMF1;PMF1-BGLAP
PMF1;PMF1-BGLAP
CUI: C2937358
Disease:
Cerebral Hemorrhage
0.700 GeneticVariation GWASDB Meta-analysis of genome-wide association studies identifies 1q22 as a susceptibility locus for intracerebral hemorrhage. 24656865 2014
dbSNP: rs6427307
rs6427307
Entrez Id: 11243;100527963
Gene Symbol: PMF1;PMF1-BGLAP
PMF1;PMF1-BGLAP
CUI: C2937358
Disease:
Cerebral Hemorrhage
0.700 GeneticVariation GWASDB Meta-analysis of genome-wide association studies identifies 1q22 as a susceptibility locus for intracerebral hemorrhage. 24656865 2014
dbSNP: rs7534434
rs7534434
Entrez Id: 11243;100527963
Gene Symbol: PMF1;PMF1-BGLAP
PMF1;PMF1-BGLAP
CUI: C2937358
Disease:
Cerebral Hemorrhage
0.700 GeneticVariation GWASDB Meta-analysis of genome-wide association studies identifies 1q22 as a susceptibility locus for intracerebral hemorrhage. 24656865 2014
dbSNP: rs887953
rs887953
Entrez Id: 11243;100527963
Gene Symbol: PMF1;PMF1-BGLAP
PMF1;PMF1-BGLAP
CUI: C2937358
Disease:
Cerebral Hemorrhage
0.700 GeneticVariation GWASDB Meta-analysis of genome-wide association studies identifies 1q22 as a susceptibility locus for intracerebral hemorrhage. 24656865 2014
dbSNP: rs1052053
rs1052053
Entrez Id: 11243;100527963
Gene Symbol: PMF1;PMF1-BGLAP
PMF1;PMF1-BGLAP
CUI: C0038454
Disease:
Cerebrovascular accident
0.700 GeneticVariation GWASCAT Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes. 29531354 2018
dbSNP: rs1052053
rs1052053
Entrez Id: 11243;100527963
Gene Symbol: PMF1;PMF1-BGLAP
PMF1;PMF1-BGLAP
CUI: C0948008
Disease:
Ischemic stroke
0.700 GeneticVariation GWASCAT Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes. 29531354 2018
dbSNP: rs2842870
rs2842870
Entrez Id: 11243;100527963
Gene Symbol: PMF1;PMF1-BGLAP
PMF1;PMF1-BGLAP
CUI: C0017654
Disease:
Glomerular Filtration Rate
T 0.700 GeneticVariation GWASCAT Trans-ethnic kidney function association study reveals putative causal genes and effects on kidney-specific disease aetiologies. 30604766 2019