RAB36, RAB36, member RAS oncogene family, 9609

N. diseases: 10; N. variants: 4
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2301555
rs2301555
Entrez Id: 9609;27156
Gene Symbol: RAB36;RSPH14
RAB36;RSPH14
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: rs4822363
rs4822363
Entrez Id: 9609;27156
Gene Symbol: RAB36;RSPH14
RAB36;RSPH14
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: rs4822363
rs4822363
Entrez Id: 9609;27156
Gene Symbol: RAB36;RSPH14
RAB36;RSPH14
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: rs5751592
rs5751592
Entrez Id: 9609;27156
Gene Symbol: RAB36;RSPH14
RAB36;RSPH14
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: rs5759603
rs5759603
Entrez Id: 9609;27156
Gene Symbol: RAB36;RSPH14
RAB36;RSPH14
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