RAB10, RAB10, member RAS oncogene family, 10890

N. diseases: 21; N. variants: 6
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2384322
rs2384322
Entrez Id: 10890
Gene Symbol: RAB10
RAB10
CUI: C1261502
Disease:
Finding of Mean Corpuscular Hemoglobin 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs10048683
rs10048683
Entrez Id: 10890
Gene Symbol: RAB10
RAB10
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: rs2243834
rs2243834
Entrez Id: 10890
Gene Symbol: RAB10
RAB10
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: rs6546744
rs6546744
Entrez Id: 10890;105374333
Gene Symbol: RAB10;LOC105374333
RAB10;LOC105374333
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: rs6546744
rs6546744
Entrez Id: 10890;105374333
Gene Symbol: RAB10;LOC105374333
RAB10;LOC105374333
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: rs6742226
rs6742226
Entrez Id: 10890
Gene Symbol: RAB10
RAB10
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: rs2243834
rs2243834
Entrez Id: 10890
Gene Symbol: RAB10
RAB10
CUI: C0524587
Disease:
Mean Corpuscular Volume (result) 		T 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs28699126
rs28699126
Entrez Id: 10890
Gene Symbol: RAB10
RAB10
CUI: C1261502
Disease:
Finding of Mean Corpuscular Hemoglobin 		T 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016