rs786205233
|
Entrez Id: |
27125 |
Gene Symbol: |
AFF4 |
AFF4
|
CHOPS SYNDROME
|
C |
0.800 |
CausalMutation |
CLINVAR |
|
|
|
rs786205679
|
Entrez Id: |
27125 |
Gene Symbol: |
AFF4 |
AFF4
|
CHOPS SYNDROME
|
C |
0.800 |
CausalMutation |
CLINVAR |
|
|
|
rs786205680
|
Entrez Id: |
27125 |
Gene Symbol: |
AFF4 |
AFF4
|
CHOPS SYNDROME
|
A |
0.800 |
GeneticVariation |
CLINVAR |
|
|
|
rs786205680
|
Entrez Id: |
27125 |
Gene Symbol: |
AFF4 |
AFF4
|
CHOPS SYNDROME
|
A |
0.800 |
CausalMutation |
CLINVAR |
Germline gain-of-function mutations in AFF4 cause a developmental syndrome functionally linking the super elongation complex and cohesin.
|
25730767 |
2015 |
rs10038027
|
Entrez Id: |
27125 |
Gene Symbol: |
AFF4 |
AFF4
|
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 |
rs10479013
|
Entrez Id: |
27125 |
Gene Symbol: |
AFF4 |
AFF4
|
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 |
rs12163971
|
Entrez Id: |
27125 |
Gene Symbol: |
AFF4 |
AFF4
|
Glomerular Filtration Rate
|
A |
0.700 |
GeneticVariation |
GWASCAT |
A catalog of genetic loci associated with kidney function from analyses of a million individuals.
|
31152163 |
2019 |
rs12653694
|
Entrez Id: |
27125 |
Gene Symbol: |
AFF4 |
AFF4
|
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 |
rs17691584
|
AFF4;ATP6V0E1P1
|
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 |
rs2525485
|
Entrez Id: |
27125 |
Gene Symbol: |
AFF4 |
AFF4
|
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 |
rs3798128
|
Entrez Id: |
27125 |
Gene Symbol: |
AFF4 |
AFF4
|
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 |
rs57880964
|
AFF4;LEAP2
|
Blood Protein Measurement
|
G |
0.700 |
GeneticVariation |
GWASCAT |
Co-regulatory networks of human serum proteins link genetics to disease.
|
30072576 |
2018 |
rs739863
|
Entrez Id: |
27125 |
Gene Symbol: |
AFF4 |
AFF4
|
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 |
rs786205233
|
Entrez Id: |
27125 |
Gene Symbol: |
AFF4 |
AFF4
|
CHOPS SYNDROME
|
|
0.800 |
GeneticVariation |
UNIPROT |
|
|
|
rs786205679
|
Entrez Id: |
27125 |
Gene Symbol: |
AFF4 |
AFF4
|
CHOPS SYNDROME
|
|
0.800 |
GeneticVariation |
UNIPROT |
|
|
|
rs786205680
|
Entrez Id: |
27125 |
Gene Symbol: |
AFF4 |
AFF4
|
CHOPS SYNDROME
|
|
0.800 |
GeneticVariation |
UNIPROT |
|
|
|