RAB38, RAB38, member RAS oncogene family, 23682

N. diseases: 34; N. variants: 17
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs302668
rs302668
Entrez Id: 23682
Gene Symbol: RAB38
RAB38
CUI: C0338451
Disease:
Frontotemporal dementia 		T 0.810 GeneticVariation GWASDB We also identified a potential novel locus at 11q14, encompassing RAB38/CTSC (the transcripts of which are related to lysosomal biology), for the behavioural FTD subtype for which joint analyses showed suggestive association for rs302668 (p=2·44 × 10(-7); 0·814 [0·71-0·92]). 24943344 2014
dbSNP: rs302668
rs302668
Entrez Id: 23682
Gene Symbol: RAB38
RAB38
CUI: C0338451
Disease:
Frontotemporal dementia 		T 0.810 GeneticVariation GWASCAT We also identified a potential novel locus at 11q14, encompassing RAB38/CTSC (the transcripts of which are related to lysosomal biology), for the behavioural FTD subtype for which joint analyses showed suggestive association for rs302668 (p=2·44 × 10(-7); 0·814 [0·71-0·92]). 24943344 2014
dbSNP: rs302668
rs302668
Entrez Id: 23682
Gene Symbol: RAB38
RAB38
CUI: C0338451
Disease:
Frontotemporal dementia 		0.810 GeneticVariation BEFREE We also identified a potential novel locus at 11q14, encompassing RAB38/CTSC (the transcripts of which are related to lysosomal biology), for the behavioural FTD subtype for which joint analyses showed suggestive association for rs302668 (p=2·44 × 10(-7); 0·814 [0·71-0·92]). 24943344 2014
dbSNP: rs116951285
rs116951285
Entrez Id: 23682
Gene Symbol: RAB38
RAB38
CUI: C0428419
Disease:
Triiodothyronine measurement 		C 0.700 GeneticVariation GWASCAT Genome-wide association meta-analysis for total thyroid hormone levels in Croatian population. 30824882 2019
dbSNP: rs10501658
rs10501658
Entrez Id: 23682
Gene Symbol: RAB38
RAB38
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: rs10831205
rs10831205
Entrez Id: 23682
Gene Symbol: RAB38
RAB38
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: rs16914161
rs16914161
Entrez Id: 23682
Gene Symbol: RAB38
RAB38
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: rs2220303
rs2220303
Entrez Id: 23682
Gene Symbol: RAB38
RAB38
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: rs534692
rs534692
Entrez Id: 23682
Gene Symbol: RAB38
RAB38
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: rs545489
rs545489
Entrez Id: 23682
Gene Symbol: RAB38
RAB38
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: rs555354
rs555354
Entrez Id: 23682
Gene Symbol: RAB38
RAB38
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: rs632483
rs632483
Entrez Id: 23682
Gene Symbol: RAB38
RAB38
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: rs642007
rs642007
Entrez Id: 23682
Gene Symbol: RAB38
RAB38
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: rs659026
rs659026
Entrez Id: 23682
Gene Symbol: RAB38
RAB38
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: rs7935712
rs7935712
Entrez Id: 23682
Gene Symbol: RAB38
RAB38
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: rs7945438
rs7945438
Entrez Id: 23682
Gene Symbol: RAB38
RAB38
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: rs953353
rs953353
Entrez Id: 23682
Gene Symbol: RAB38
RAB38
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: rs988975
rs988975
Entrez Id: 23682
Gene Symbol: RAB38
RAB38
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: rs9144
rs9144
Entrez Id: 23682
Gene Symbol: RAB38
RAB38
CUI: C0010346
Disease:
Crohn Disease 		0.010 GeneticVariation BEFREE In addition, the Crohn's disease activity index at the first infliximab use and rs9144 (P = 0.001) were independently associated with the loss of response in patients with Crohn's disease. 30851117 2019
dbSNP: rs302668
rs302668
Entrez Id: 23682
Gene Symbol: RAB38
RAB38
CUI: C0002395
Disease:
Alzheimer's Disease 		0.010 GeneticVariation BEFREE The SNPs rs302668 in RAB38, rs9268877 and rs9268856 polymorphism in HLA-DRA/HLA-DRB5, and rs1980493 polymorphism in BTNL2 might play a role in the susceptibility to late-onset AD in the Han Chinese population. 26967218 2016