rs10501658
×
Entrez Id:
23682
Gene Symbol:
RAB38
RAB38
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
rs10831205
×
Entrez Id:
23682
Gene Symbol:
RAB38
RAB38
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
rs116951285
×
Entrez Id:
23682
Gene Symbol:
RAB38
RAB38
Triiodothyronine measurement
C
0.700
GeneticVariation
GWASCAT
Genome-wide association meta-analysis for total thyroid hormone levels in Croatian population.
30824882
2019
rs16914161
×
Entrez Id:
23682
Gene Symbol:
RAB38
RAB38
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
rs2220303
×
Entrez Id:
23682
Gene Symbol:
RAB38
RAB38
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
rs302668
×
Entrez Id:
23682
Gene Symbol:
RAB38
RAB38
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
rs302668
×
Entrez Id:
23682
Gene Symbol:
RAB38
RAB38
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
rs302668
×
Entrez Id:
23682
Gene Symbol:
RAB38
RAB38
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
rs302668
×
Entrez Id:
23682
Gene Symbol:
RAB38
RAB38
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
rs534692
×
Entrez Id:
23682
Gene Symbol:
RAB38
RAB38
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
rs545489
×
Entrez Id:
23682
Gene Symbol:
RAB38
RAB38
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
rs555354
×
Entrez Id:
23682
Gene Symbol:
RAB38
RAB38
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
rs632483
×
Entrez Id:
23682
Gene Symbol:
RAB38
RAB38
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
rs642007
×
Entrez Id:
23682
Gene Symbol:
RAB38
RAB38
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
rs659026
×
Entrez Id:
23682
Gene Symbol:
RAB38
RAB38
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
rs7935712
×
Entrez Id:
23682
Gene Symbol:
RAB38
RAB38
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
rs7945438
×
Entrez Id:
23682
Gene Symbol:
RAB38
RAB38
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
rs9144
×
Entrez Id:
23682
Gene Symbol:
RAB38
RAB38
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
rs953353
×
Entrez Id:
23682
Gene Symbol:
RAB38
RAB38
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
rs988975
×
Entrez Id:
23682
Gene Symbol:
RAB38
RAB38
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