RAB5C, RAB5C, member RAS oncogene family, 5878

N. diseases: 24; N. variants: 18
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs11079035
rs11079035
Entrez Id: 5878
Gene Symbol: RAB5C
RAB5C
CUI: C0023508
Disease:
White Blood Cell Count procedure 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs12325861
rs12325861
Entrez Id: 5878
Gene Symbol: RAB5C
RAB5C
CUI: C0020676
Disease:
Hypothyroidism 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs13380830
rs13380830
Entrez Id: 5878
Gene Symbol: RAB5C
RAB5C
CUI: C0004364
Disease:
Autoimmune Diseases 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs13380830
rs13380830
Entrez Id: 5878
Gene Symbol: RAB5C
RAB5C
CUI: C4310768
Disease:
AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 2 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs13380830
rs13380830
Entrez Id: 5878
Gene Symbol: RAB5C
RAB5C
CUI: C4014795
Disease:
AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 1 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs13380830
rs13380830
Entrez Id: 5878
Gene Symbol: RAB5C
RAB5C
CUI: C3150797
Disease:
AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 6 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs1869365
rs1869365
Entrez Id: 5878
Gene Symbol: RAB5C
RAB5C
CUI: C2239219
Disease:
von Willebrand's factor (lab test) 		0.700 GeneticVariation GWASCAT Genome-Wide Association Transethnic Meta-Analyses Identifies Novel Associations Regulating Coagulation Factor VIII and von Willebrand Factor Plasma Levels. 30586737 2019
dbSNP: rs1869365
rs1869365
Entrez Id: 5878
Gene Symbol: RAB5C
RAB5C
CUI: C2825857
Disease:
Factor VIII measurement 		0.700 GeneticVariation GWASCAT Genome-Wide Association Transethnic Meta-Analyses Identifies Novel Associations Regulating Coagulation Factor VIII and von Willebrand Factor Plasma Levels. 30586737 2019
dbSNP: rs78862468
rs78862468
Entrez Id: 5878
Gene Symbol: RAB5C
RAB5C
CUI: C1261502
Disease:
Finding of Mean Corpuscular Hemoglobin 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs7224737
rs7224737
Entrez Id: 5878
Gene Symbol: RAB5C
RAB5C
CUI: C0337428
Disease:
Fibrinogen assay 		0.700 GeneticVariation GWASCAT Comparison of HapMap and 1000 Genomes Reference Panels in a Large-Scale Genome-Wide Association Study. 28107422 2017
dbSNP: rs11079035
rs11079035
Entrez Id: 5878
Gene Symbol: RAB5C
RAB5C
CUI: C0042900
Disease:
Vitiligo 		A 0.700 GeneticVariation GWASCAT Genome-wide association studies of autoimmune vitiligo identify 23 new risk loci and highlight key pathways and regulatory variants. 27723757 2016
dbSNP: rs7224737
rs7224737
Entrez Id: 5878
Gene Symbol: RAB5C
RAB5C
CUI: C0337428
Disease:
Fibrinogen assay 		A 0.700 GeneticVariation GWASCAT A meta-analysis of 120 246 individuals identifies 18 new loci for fibrinogen concentration. 26561523 2016
dbSNP: rs11079034
rs11079034
Entrez Id: 5878
Gene Symbol: RAB5C
RAB5C
CUI: C0523465
Disease:
Serum albumin measurement 		0.700 GeneticVariation GWASDB A genome-wide assessment of variability in human serum metabolism. 23281178 2013
dbSNP: rs11079035
rs11079035
Entrez Id: 5878
Gene Symbol: RAB5C
RAB5C
CUI: C0523465
Disease:
Serum albumin measurement 		0.700 GeneticVariation GWASDB A genome-wide assessment of variability in human serum metabolism. 23281178 2013
dbSNP: rs12603327
rs12603327
Entrez Id: 5878
Gene Symbol: RAB5C
RAB5C
CUI: C0523465
Disease:
Serum albumin measurement 		0.700 GeneticVariation GWASDB A genome-wide assessment of variability in human serum metabolism. 23281178 2013
dbSNP: rs12603330
rs12603330
Entrez Id: 5878
Gene Symbol: RAB5C
RAB5C
CUI: C0523465
Disease:
Serum albumin measurement 		0.700 GeneticVariation GWASDB A genome-wide assessment of variability in human serum metabolism. 23281178 2013
dbSNP: rs2240009
rs2240009
Entrez Id: 5878
Gene Symbol: RAB5C
RAB5C
CUI: C0523465
Disease:
Serum albumin measurement 		0.700 GeneticVariation GWASDB A genome-wide assessment of variability in human serum metabolism. 23281178 2013
dbSNP: rs7214921
rs7214921
Entrez Id: 5878
Gene Symbol: RAB5C
RAB5C
CUI: C0523465
Disease:
Serum albumin measurement 		0.700 GeneticVariation GWASDB A genome-wide assessment of variability in human serum metabolism. 23281178 2013
dbSNP: rs7224737
rs7224737
Entrez Id: 5878
Gene Symbol: RAB5C
RAB5C
CUI: C0523465
Disease:
Serum albumin measurement 		0.700 GeneticVariation GWASDB A genome-wide assessment of variability in human serum metabolism. 23281178 2013
dbSNP: rs739636
rs739636
Entrez Id: 5878
Gene Symbol: RAB5C
RAB5C
CUI: C0523465
Disease:
Serum albumin measurement 		0.700 GeneticVariation GWASDB A genome-wide assessment of variability in human serum metabolism. 23281178 2013
dbSNP: rs739637
rs739637
Entrez Id: 5878
Gene Symbol: RAB5C
RAB5C
CUI: C0523465
Disease:
Serum albumin measurement 		0.700 GeneticVariation GWASDB A genome-wide assessment of variability in human serum metabolism. 23281178 2013
dbSNP: rs8070446
rs8070446
Entrez Id: 5878
Gene Symbol: RAB5C
RAB5C
CUI: C0523465
Disease:
Serum albumin measurement 		0.700 GeneticVariation GWASDB A genome-wide assessment of variability in human serum metabolism. 23281178 2013
dbSNP: rs8074708
rs8074708
Entrez Id: 5878
Gene Symbol: RAB5C
RAB5C
CUI: C0523465
Disease:
Serum albumin measurement 		0.700 GeneticVariation GWASDB A genome-wide assessment of variability in human serum metabolism. 23281178 2013
dbSNP: rs9903204
rs9903204
Entrez Id: 5878
Gene Symbol: RAB5C
RAB5C
CUI: C0523465
Disease:
Serum albumin measurement 		0.700 GeneticVariation GWASDB A genome-wide assessment of variability in human serum metabolism. 23281178 2013
dbSNP: rs9915255
rs9915255
Entrez Id: 5878
Gene Symbol: RAB5C
RAB5C
CUI: C0523465
Disease:
Serum albumin measurement 		0.700 GeneticVariation GWASDB A genome-wide assessment of variability in human serum metabolism. 23281178 2013