PDLIM5, PDZ and LIM domain 5, 10611

N. diseases: 148; N. variants: 19
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs4699299
rs4699299
Entrez Id: 10611
Gene Symbol: PDLIM5
PDLIM5
CUI: C0042133
Disease:
Uterine Fibroids
T 0.700 GeneticVariation GWASCAT Genome-wide association and epidemiological analyses reveal common genetic origins between uterine leiomyomata and endometriosis. 31649266 2019
dbSNP: rs4699299
rs4699299
Entrez Id: 10611
Gene Symbol: PDLIM5
PDLIM5
CUI: C2242776
Disease:
Plexiform leiomyoma
T 0.700 GeneticVariation GWASCAT Genome-wide association and epidemiological analyses reveal common genetic origins between uterine leiomyomata and endometriosis. 31649266 2019
dbSNP: rs17021918
rs17021918
Entrez Id: 10611
Gene Symbol: PDLIM5
PDLIM5
CUI: C0600139
Disease:
Prostate carcinoma
C 0.700 GeneticVariation GWASCAT Association analyses of more than 140,000 men identify 63 new prostate cancer susceptibility loci. 29892016 2018
dbSNP: rs2452600
rs2452600
Entrez Id: 10611
Gene Symbol: PDLIM5
PDLIM5
CUI: C1956346
Disease:
Coronary Artery Disease
T 0.700 GeneticVariation GWASCAT Identification of 64 Novel Genetic Loci Provides an Expanded View on the Genetic Architecture of Coronary Artery Disease. 29212778 2018
dbSNP: rs11731606
rs11731606
Entrez Id: 10611
Gene Symbol: PDLIM5
PDLIM5
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: rs200495769
rs200495769
Entrez Id: 10611
Gene Symbol: PDLIM5
PDLIM5
CUI: C1961102
Disease:
Precursor Cell Lymphoblastic Leukemia Lymphoma
T 0.700 GeneticVariation GWASCAT Clinical and Genetic Risk Factors for Acute Pancreatitis in Patients With Acute Lymphoblastic Leukemia. 27114598 2016
dbSNP: rs12500426
rs12500426
Entrez Id: 10611
Gene Symbol: PDLIM5
PDLIM5
CUI: C2931822
Disease:
Nasopharyngeal carcinoma
0.700 GeneticVariation GWASDB A genome-wide association study of nasopharyngeal carcinoma identifies three new susceptibility loci. 20512145 2010
dbSNP: rs17021918
rs17021918
Entrez Id: 10611
Gene Symbol: PDLIM5
PDLIM5
CUI: C2931822
Disease:
Nasopharyngeal carcinoma
0.700 GeneticVariation GWASDB A genome-wide association study of nasopharyngeal carcinoma identifies three new susceptibility loci. 20512145 2010
dbSNP: rs12500426
rs12500426
Entrez Id: 10611
Gene Symbol: PDLIM5
PDLIM5
CUI: C0376358
Disease:
Malignant neoplasm of prostate
A 0.700 GeneticVariation GWASDB Identification of seven new prostate cancer susceptibility loci through a genome-wide association study. 19767753 2009
dbSNP: rs12500426
rs12500426
Entrez Id: 10611
Gene Symbol: PDLIM5
PDLIM5
CUI: C0600139
Disease:
Prostate carcinoma
0.700 GeneticVariation GWASCAT Identification of seven new prostate cancer susceptibility loci through a genome-wide association study. 19767753 2009
dbSNP: rs17021918
rs17021918
Entrez Id: 10611
Gene Symbol: PDLIM5
PDLIM5
CUI: C0600139
Disease:
Prostate carcinoma
0.700 GeneticVariation GWASCAT Identification of seven new prostate cancer susceptibility loci through a genome-wide association study. 19767753 2009
dbSNP: rs17021918
rs17021918
Entrez Id: 10611
Gene Symbol: PDLIM5
PDLIM5
CUI: C0376358
Disease:
Malignant neoplasm of prostate
T 0.700 GeneticVariation GWASDB Identification of seven new prostate cancer susceptibility loci through a genome-wide association study. 19767753 2009
dbSNP: rs2433322
rs2433322
Entrez Id: 10611
Gene Symbol: PDLIM5
PDLIM5
CUI: C0036341
Disease:
Schizophrenia
0.020 GeneticVariation BEFREE In addition, high linkage disequilibrium was observed between rs2433320 and rs2433322 (D'=0.880), and haplotypes constructed from the two SNPs were significantly associated with schizophrenia (global P=0.00019, even after strict Bonferroni correction). 18021463 2008
dbSNP: rs2433322
rs2433322
Entrez Id: 10611
Gene Symbol: PDLIM5
PDLIM5
CUI: C0036341
Disease:
Schizophrenia
0.020 GeneticVariation BEFREE We identified 27 polymorphisms in PDLIM5 and found associations between polymorphisms (rs2433320 and rs2433322) in the 5' region of the gene and schizophrenia (p = .004). 16213469 2006
dbSNP: rs11097432
rs11097432
Entrez Id: 10611
Gene Symbol: PDLIM5
PDLIM5
CUI: C0011860
Disease:
Diabetes Mellitus, Non-Insulin-Dependent
0.010 GeneticVariation BEFREE Of the 25 SNPs, 5 SNPs showed associations with both AD in the SAGE sample and T2D in the Marshfield sample (top SNP rs11097432 with p = 0.00107 for T2D and p = 0.0483 for AD) while 6 SNPs showed associations with both AD in the SAGE sample and hypertension in the Marshfield sample (top SNP rs12500426 with p = 0.0119 for hypertension and p = 1.51 × 10<sup>-3</sup> for AD). 27693979 2017
dbSNP: rs11097432
rs11097432
Entrez Id: 10611
Gene Symbol: PDLIM5
PDLIM5
CUI: C0020538
Disease:
Hypertensive disease
0.010 GeneticVariation BEFREE Of the 25 SNPs, 5 SNPs showed associations with both AD in the SAGE sample and T2D in the Marshfield sample (top SNP rs11097432 with p = 0.00107 for T2D and p = 0.0483 for AD) while 6 SNPs showed associations with both AD in the SAGE sample and hypertension in the Marshfield sample (top SNP rs12500426 with p = 0.0119 for hypertension and p = 1.51 × 10<sup>-3</sup> for AD). 27693979 2017
dbSNP: rs12500426
rs12500426
Entrez Id: 10611
Gene Symbol: PDLIM5
PDLIM5
CUI: C0011860
Disease:
Diabetes Mellitus, Non-Insulin-Dependent
0.010 GeneticVariation BEFREE Of the 25 SNPs, 5 SNPs showed associations with both AD in the SAGE sample and T2D in the Marshfield sample (top SNP rs11097432 with p = 0.00107 for T2D and p = 0.0483 for AD) while 6 SNPs showed associations with both AD in the SAGE sample and hypertension in the Marshfield sample (top SNP rs12500426 with p = 0.0119 for hypertension and p = 1.51 × 10<sup>-3</sup> for AD). 27693979 2017
dbSNP: rs12500426
rs12500426
Entrez Id: 10611
Gene Symbol: PDLIM5
PDLIM5
CUI: C0020538
Disease:
Hypertensive disease
0.010 GeneticVariation BEFREE Of the 25 SNPs, 5 SNPs showed associations with both AD in the SAGE sample and T2D in the Marshfield sample (top SNP rs11097432 with p = 0.00107 for T2D and p = 0.0483 for AD) while 6 SNPs showed associations with both AD in the SAGE sample and hypertension in the Marshfield sample (top SNP rs12500426 with p = 0.0119 for hypertension and p = 1.51 × 10<sup>-3</sup> for AD). 27693979 2017
dbSNP: rs6532496
rs6532496
Entrez Id: 10611
Gene Symbol: PDLIM5
PDLIM5
CUI: C0020538
Disease:
Hypertensive disease
0.010 GeneticVariation BEFREE SNP (rs6532496) showed significant interaction with alcohol consumption for hypertension. 27693979 2017
dbSNP: rs368434732
rs368434732
Entrez Id: 10611
Gene Symbol: PDLIM5
PDLIM5
CUI: C2678065
Disease:
Myofibrillar Myopathy
0.010 GeneticVariation BEFREE The c.626 C > T (p.P209L) mutation in the BAG3 gene has been described as causative of a subtype of MFM. 27443559 2016
dbSNP: rs11097431
rs11097431
Entrez Id: 10611
Gene Symbol: PDLIM5
PDLIM5
CUI: C0036341
Disease:
Schizophrenia
0.010 GeneticVariation BEFREE However, no association was detected between the rs11097431 polymorphism either with bipolar disorder or with schizophrenia. 24064681 2013
dbSNP: rs11097431
rs11097431
Entrez Id: 10611
Gene Symbol: PDLIM5
PDLIM5
CUI: C0005586
Disease:
Bipolar Disorder
0.010 GeneticVariation BEFREE However, no association was detected between the rs11097431 polymorphism either with bipolar disorder or with schizophrenia. 24064681 2013
dbSNP: rs17021918
rs17021918
Entrez Id: 10611
Gene Symbol: PDLIM5
PDLIM5
CUI: C0006142
Disease:
Malignant neoplasm of breast
0.010 GeneticVariation BEFREE Four SNPs were associated with aggressive PrCa, while three other SNPs showed potential interactions for PrCa by family history of PrCa (rs8102476; 19q13), lung cancer (rs17021918; 4q22), and breast cancer (rs10896449; 11q13). 23573233 2013
dbSNP: rs17021918
rs17021918
Entrez Id: 10611
Gene Symbol: PDLIM5
PDLIM5
CUI: C0678222
Disease:
Breast Carcinoma
0.010 GeneticVariation BEFREE Four SNPs were associated with aggressive PrCa, while three other SNPs showed potential interactions for PrCa by family history of PrCa (rs8102476; 19q13), lung cancer (rs17021918; 4q22), and breast cancer (rs10896449; 11q13). 23573233 2013
dbSNP: rs17021918
rs17021918
Entrez Id: 10611
Gene Symbol: PDLIM5
PDLIM5
CUI: C1306460
Disease:
Primary malignant neoplasm of lung
0.010 GeneticVariation BEFREE Four SNPs were associated with aggressive PrCa, while three other SNPs showed potential interactions for PrCa by family history of PrCa (rs8102476; 19q13), lung cancer (rs17021918; 4q22), and breast cancer (rs10896449; 11q13). 23573233 2013