DLC1, DLC1 Rho GTPase activating protein, 10395

N. diseases: 144; N. variants: 21
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs117489831
rs117489831
Entrez Id: 10395
Gene Symbol: DLC1
DLC1
CUI: C0005890
Disease:
Body Height 		0.700 GeneticVariation GWASCAT Characterizing rare and low-frequency height-associated variants in the Japanese population. 31562340 2019
dbSNP: rs118111862
rs118111862
Entrez Id: 10395
Gene Symbol: DLC1
DLC1
CUI: C0014772
Disease:
Red Blood Cell Count measurement 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs118111862
rs118111862
Entrez Id: 10395
Gene Symbol: DLC1
DLC1
CUI: C1261502
Disease:
Finding of Mean Corpuscular Hemoglobin 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs28539528
rs28539528
Entrez Id: 10395
Gene Symbol: DLC1
DLC1
CUI: C0023508
Disease:
White Blood Cell Count procedure 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs59738387
rs59738387
Entrez Id: 10395;101930149
Gene Symbol: DLC1;LOC101930149
DLC1;LOC101930149
CUI: C0005890
Disease:
Body Height 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs76364830
rs76364830
Entrez Id: 10395
Gene Symbol: DLC1
DLC1
CUI: C0005890
Disease:
Body Height 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs1160554
rs1160554
Entrez Id: 10395
Gene Symbol: DLC1
DLC1
CUI: C0040420
Disease:
Tonometry 		C 0.700 GeneticVariation GWASCAT Genome-wide association analyses identify new loci influencing intraocular pressure. 29617998 2018
dbSNP: rs12548673
rs12548673
Entrez Id: 10395
Gene Symbol: DLC1
DLC1
CUI: C0040420
Disease:
Tonometry 		0.700 GeneticVariation GWASCAT Genome-wide association study of intraocular pressure uncovers new pathways to glaucoma. 30054594 2018
dbSNP: rs6993558
rs6993558
Entrez Id: 10395
Gene Symbol: DLC1
DLC1
CUI: C0205682
Disease:
Waist-Hip Ratio 		T 0.700 GeneticVariation GWASCAT Whole-Genome Sequencing Coupled to Imputation Discovers Genetic Signals for Anthropometric Traits. 28552196 2017
dbSNP: rs77236434
rs77236434
Entrez Id: 10395
Gene Symbol: DLC1
DLC1
CUI: C2239176
Disease:
Liver carcinoma 		T 0.700 GeneticVariation GWASCAT Genome-wide association analysis identifies a GLUL haplotype for familial hepatitis B virus-related hepatocellular carcinoma. 28662289 2017
dbSNP: rs77236434
rs77236434
Entrez Id: 10395
Gene Symbol: DLC1
DLC1
CUI: C0019163
Disease:
Hepatitis B 		T 0.700 GeneticVariation GWASCAT Genome-wide association analysis identifies a GLUL haplotype for familial hepatitis B virus-related hepatocellular carcinoma. 28662289 2017
dbSNP: rs12541254
rs12541254
Entrez Id: 10395
Gene Symbol: DLC1
DLC1
CUI: C1861172
Disease:
Venous Thromboembolism 		A 0.700 GeneticVariation GWASDB A genome-wide search for common SNP x SNP interactions on the risk of venous thrombosis. 23509962 2013
dbSNP: rs17793145
rs17793145
Entrez Id: 10395
Gene Symbol: DLC1
DLC1
CUI: C0036341
Disease:
Schizophrenia 		0.700 GeneticVariation GWASDB Genome-wide association study identifies five new schizophrenia loci. 21926974 2011
dbSNP: rs121908500
rs121908500
Entrez Id: 10395
Gene Symbol: DLC1
DLC1
CUI: C0009402
Disease:
Colorectal Carcinoma 		C 0.700 CausalMutation CLINVAR
dbSNP: rs1303000329
rs1303000329
Entrez Id: 10395
Gene Symbol: DLC1
DLC1
CUI: C0080174
Disease:
Spina Bifida Occulta 		A 0.700 SusceptibilityMutation CLINVAR
dbSNP: rs1303000329
rs1303000329
Entrez Id: 10395
Gene Symbol: DLC1
DLC1
CUI: C0086664
Disease:
Myelocele 		A 0.700 SusceptibilityMutation CLINVAR
dbSNP: rs1303000329
rs1303000329
Entrez Id: 10395
Gene Symbol: DLC1
DLC1
CUI: C3891448
Disease:
NEURAL TUBE DEFECTS, SUSCEPTIBILITY TO 		A 0.700 SusceptibilityMutation CLINVAR
dbSNP: rs1303000329
rs1303000329
Entrez Id: 10395
Gene Symbol: DLC1
DLC1
CUI: C0025312
Disease:
Meningomyelocele 		A 0.700 SusceptibilityMutation CLINVAR
dbSNP: rs1563593163
rs1563593163
Entrez Id: 10395
Gene Symbol: DLC1
DLC1
CUI: C0025312
Disease:
Meningomyelocele 		A 0.700 SusceptibilityMutation CLINVAR
dbSNP: rs1563593163
rs1563593163
Entrez Id: 10395
Gene Symbol: DLC1
DLC1
CUI: C3891448
Disease:
NEURAL TUBE DEFECTS, SUSCEPTIBILITY TO 		A 0.700 SusceptibilityMutation CLINVAR
dbSNP: rs621554
rs621554
Entrez Id: 10395
Gene Symbol: DLC1
DLC1
CUI: C0678222
Disease:
Breast Carcinoma 		0.010 GeneticVariation BEFREE These results suggested that the rs621554 polymorphism is associated with breast cancer susceptibility and prognosis, and may serve as a biomarker for breast cancer development and progression. 26986853 2016
dbSNP: rs621554
rs621554
Entrez Id: 10395
Gene Symbol: DLC1
DLC1
CUI: C2239176
Disease:
Liver carcinoma 		0.010 GeneticVariation BEFREE The rs621554 (IVS19+108C>T) polymorphism is a synonymous single nucleotide polymorphism (SNP) previously found to be associated with hepatocellular carcinoma. 26986853 2016
dbSNP: rs621554
rs621554
Entrez Id: 10395
Gene Symbol: DLC1
DLC1
CUI: C0006142
Disease:
Malignant neoplasm of breast 		0.010 GeneticVariation BEFREE These results suggested that the rs621554 polymorphism is associated with breast cancer susceptibility and prognosis, and may serve as a biomarker for breast cancer development and progression. 26986853 2016
dbSNP: rs11203495
rs11203495
Entrez Id: 10395
Gene Symbol: DLC1
DLC1
CUI: C0027651
Disease:
Neoplasms 		0.010 GeneticVariation BEFREE Furthermore, patients with the GC+CC genotype of rs3816748, the TC+CC genotype of rs11203495 or the GA+AA genotype of rs3816747 had small‑sized tumors compared with those carrying the wild‑type genotype. 26095787 2015
dbSNP: rs3816747
rs3816747
Entrez Id: 10395
Gene Symbol: DLC1
DLC1
CUI: C0027651
Disease:
Neoplasms 		0.010 GeneticVariation BEFREE Furthermore, patients with the GC+CC genotype of rs3816748, the TC+CC genotype of rs11203495 or the GA+AA genotype of rs3816747 had small‑sized tumors compared with those carrying the wild‑type genotype. 26095787 2015