PDZRN3, PDZ domain containing ring finger 3, 23024

N. diseases: 11; N. variants: 14
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs4461368
rs4461368
Entrez Id: 23024;101927296
Gene Symbol: PDZRN3;LOC101927296
PDZRN3;LOC101927296
CUI: C0429087
Disease:
Electrocardiogram: P-R interval 		T 0.700 GeneticVariation GWASCAT Genome-wide association meta-analysis of 30,000 samples identifies seven novel loci for quantitative ECG traits. 30679814 2019
dbSNP: rs13087058
rs13087058
Entrez Id: 23024
Gene Symbol: PDZRN3
PDZRN3
CUI: C0429087
Disease:
Electrocardiogram: P-R interval 		C 0.700 GeneticVariation GWASCAT PR interval genome-wide association meta-analysis identifies 50 loci associated with atrial and atrioventricular electrical activity. 30046033 2018
dbSNP: rs11709074
rs11709074
Entrez Id: 23024
Gene Symbol: PDZRN3
PDZRN3
CUI: C0023467
Disease:
Leukemia, Myelocytic, Acute 		T 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959 2017
dbSNP: rs11915881
rs11915881
Entrez Id: 23024
Gene Symbol: PDZRN3
PDZRN3
CUI: C0023467
Disease:
Leukemia, Myelocytic, Acute 		T 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959 2017
dbSNP: rs1565176
rs1565176
Entrez Id: 23024
Gene Symbol: PDZRN3
PDZRN3
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: rs1565176
rs1565176
Entrez Id: 23024
Gene Symbol: PDZRN3
PDZRN3
CUI: C0023467
Disease:
Leukemia, Myelocytic, Acute 		G 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959 2017
dbSNP: rs17703683
rs17703683
Entrez Id: 23024
Gene Symbol: PDZRN3
PDZRN3
CUI: C0023467
Disease:
Leukemia, Myelocytic, Acute 		C 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959 2017
dbSNP: rs6549543
rs6549543
Entrez Id: 23024
Gene Symbol: PDZRN3
PDZRN3
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: rs6769380
rs6769380
Entrez Id: 23024
Gene Symbol: PDZRN3
PDZRN3
CUI: C0023467
Disease:
Leukemia, Myelocytic, Acute 		T 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959 2017
dbSNP: rs6784863
rs6784863
Entrez Id: 23024
Gene Symbol: PDZRN3
PDZRN3
CUI: C0023467
Disease:
Leukemia, Myelocytic, Acute 		G 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959 2017
dbSNP: rs7651823
rs7651823
Entrez Id: 23024
Gene Symbol: PDZRN3
PDZRN3
CUI: C0023467
Disease:
Leukemia, Myelocytic, Acute 		C 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959 2017
dbSNP: rs748809996
rs748809996
Entrez Id: 23024
Gene Symbol: PDZRN3
PDZRN3
CUI: C0036346
Disease:
Schizophrenia, Childhood 		T 0.700 GeneticVariation CLINVAR De novo variants in sporadic cases of childhood onset schizophrenia. 26508570 2016
dbSNP: rs11128347
rs11128347
Entrez Id: 23024
Gene Symbol: PDZRN3
PDZRN3
CUI: C0022661
Disease:
Kidney Failure, Chronic 		0.700 GeneticVariation GWASCAT Genome-wide association scan for survival on dialysis in African-Americans with type 2 diabetes. 21546767 2011
dbSNP: rs747762087
rs747762087
Entrez Id: 23024
Gene Symbol: PDZRN3
PDZRN3
CUI: C0349588
Disease:
Short stature 		G 0.700 GeneticVariation CLINVAR
dbSNP: rs778037798
rs778037798
Entrez Id: 23024
Gene Symbol: PDZRN3
PDZRN3
CUI: C0349588
Disease:
Short stature 		G 0.700 GeneticVariation CLINVAR