rs6742445
×
Entrez Id:
55120
Gene Symbol:
FANCL
FANCL
HIV-1, RESISTANCE TO
T
0.700
GeneticVariation
GWASCAT
Association Between Single-Nucleotide Polymorphisms in HLA Alleles and Human Immunodeficiency Virus Type 1 Viral Load in Demographically Diverse, Antiretroviral Therapy-Naive Participants From the Strategic Timing of AntiRetroviral Treatment Trial.
31219150
2019
rs6742445
×
Entrez Id:
55120
Gene Symbol:
FANCL
FANCL
ACQUIRED IMMUNODEFICIENCY SYNDROME, PROGRESSION TO
T
0.700
GeneticVariation
GWASCAT
Association Between Single-Nucleotide Polymorphisms in HLA Alleles and Human Immunodeficiency Virus Type 1 Viral Load in Demographically Diverse, Antiretroviral Therapy-Naive Participants From the Strategic Timing of AntiRetroviral Treatment Trial.
31219150
2019
rs6742445
×
Entrez Id:
55120
Gene Symbol:
FANCL
FANCL
HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, SUSCEPTIBILITY TO
T
0.700
GeneticVariation
GWASCAT
Association Between Single-Nucleotide Polymorphisms in HLA Alleles and Human Immunodeficiency Virus Type 1 Viral Load in Demographically Diverse, Antiretroviral Therapy-Naive Participants From the Strategic Timing of AntiRetroviral Treatment Trial.
31219150
2019
rs6742445
×
Entrez Id:
55120
Gene Symbol:
FANCL
FANCL
AIDS, PROGRESSION TO
T
0.700
GeneticVariation
GWASCAT
Association Between Single-Nucleotide Polymorphisms in HLA Alleles and Human Immunodeficiency Virus Type 1 Viral Load in Demographically Diverse, Antiretroviral Therapy-Naive Participants From the Strategic Timing of AntiRetroviral Treatment Trial.
31219150
2019
rs6742445
×
Entrez Id:
55120
Gene Symbol:
FANCL
FANCL
Viral Load result
T
0.700
GeneticVariation
GWASCAT
Association Between Single-Nucleotide Polymorphisms in HLA Alleles and Human Immunodeficiency Virus Type 1 Viral Load in Demographically Diverse, Antiretroviral Therapy-Naive Participants From the Strategic Timing of AntiRetroviral Treatment Trial.
31219150
2019
rs747253294
VRK2;FANCL
Fanconi Anemia
C
0.700
GeneticVariation
CLINVAR
Evaluation of ACMG-Guideline-Based Variant Classification of Cancer Susceptibility and Non-Cancer-Associated Genes in Families Affected by Breast Cancer.
27153395
2016
rs747253294
VRK2;FANCL
FANCONI ANEMIA, COMPLEMENTATION GROUP L
C
0.700
GeneticVariation
CLINVAR
Evaluation of ACMG-Guideline-Based Variant Classification of Cancer Susceptibility and Non-Cancer-Associated Genes in Families Affected by Breast Cancer.
27153395
2016
rs747253294
VRK2;FANCL
FANCONI ANEMIA, COMPLEMENTATION GROUP L
C
0.700
GeneticVariation
CLINVAR
Genomic analysis of bone marrow failure and myelodysplastic syndromes reveals phenotypic and diagnostic complexity.
25239263
2015
rs747253294
VRK2;FANCL
FANCONI ANEMIA, COMPLEMENTATION GROUP L
C
0.700
GeneticVariation
CLINVAR
FANCD2, FANCJ and BRCA2 cooperate to promote replication fork recovery independently of the Fanconi Anemia core complex.
25659033
2015
rs750871999
VRK2;FANCL
Fanconi Anemia
A
0.700
GeneticVariation
CLINVAR
Structure of the human FANCL RING-Ube2T complex reveals determinants of cognate E3-E2 selection.
24389026
2014
rs1205006300
×
Entrez Id:
55120
Gene Symbol:
FANCL
FANCL
Fanconi Anemia
A
0.700
GeneticVariation
CLINVAR
Massively parallel sequencing, aCGH, and RNA-Seq technologies provide a comprehensive molecular diagnosis of Fanconi anemia.
23613520
2013
rs144729980
×
Entrez Id:
55120
Gene Symbol:
FANCL
FANCL
Fanconi Anemia
T
0.700
GeneticVariation
CLINVAR
Massively parallel sequencing, aCGH, and RNA-Seq technologies provide a comprehensive molecular diagnosis of Fanconi anemia.
23613520
2013
rs1558727300
VRK2;FANCL
Fanconi Anemia
G
0.700
GeneticVariation
CLINVAR
Massively parallel sequencing, aCGH, and RNA-Seq technologies provide a comprehensive molecular diagnosis of Fanconi anemia.
23613520
2013
rs1558737575
VRK2;FANCL
Fanconi Anemia
C
0.700
GeneticVariation
CLINVAR
Massively parallel sequencing, aCGH, and RNA-Seq technologies provide a comprehensive molecular diagnosis of Fanconi anemia.
23613520
2013
rs747253294
VRK2;FANCL
Fanconi Anemia
C
0.700
GeneticVariation
CLINVAR
Massively parallel sequencing, aCGH, and RNA-Seq technologies provide a comprehensive molecular diagnosis of Fanconi anemia.
23613520
2013
rs747253294
VRK2;FANCL
FANCONI ANEMIA, COMPLEMENTATION GROUP L
C
0.700
GeneticVariation
CLINVAR
Massively parallel sequencing, aCGH, and RNA-Seq technologies provide a comprehensive molecular diagnosis of Fanconi anemia.
23613520
2013
rs1205006300
×
Entrez Id:
55120
Gene Symbol:
FANCL
FANCL
Fanconi Anemia
A
0.700
GeneticVariation
CLINVAR
Identification and characterization of mutations in FANCL gene: a second case of Fanconi anemia belonging to FA-L complementation group.
19405097
2009
rs144729980
×
Entrez Id:
55120
Gene Symbol:
FANCL
FANCL
Fanconi Anemia
T
0.700
GeneticVariation
CLINVAR
Identification and characterization of mutations in FANCL gene: a second case of Fanconi anemia belonging to FA-L complementation group.
19405097
2009
rs1558727300
VRK2;FANCL
Fanconi Anemia
G
0.700
GeneticVariation
CLINVAR
Identification and characterization of mutations in FANCL gene: a second case of Fanconi anemia belonging to FA-L complementation group.
19405097
2009
rs1558737575
VRK2;FANCL
Fanconi Anemia
C
0.700
GeneticVariation
CLINVAR
Identification and characterization of mutations in FANCL gene: a second case of Fanconi anemia belonging to FA-L complementation group.
19405097
2009
rs747253294
VRK2;FANCL
FANCONI ANEMIA, COMPLEMENTATION GROUP L
C
0.700
GeneticVariation
CLINVAR
Identification and characterization of mutations in FANCL gene: a second case of Fanconi anemia belonging to FA-L complementation group.
19405097
2009
rs747253294
VRK2;FANCL
Fanconi Anemia
C
0.700
GeneticVariation
CLINVAR
Identification and characterization of mutations in FANCL gene: a second case of Fanconi anemia belonging to FA-L complementation group.
19405097
2009
rs750871999
VRK2;FANCL
Fanconi Anemia
A
0.700
GeneticVariation
CLINVAR
Mechanistic insight into site-restricted monoubiquitination of FANCD2 by Ube2t, FANCL, and FANCI.
19111657
2008
rs750871999
VRK2;FANCL
Fanconi Anemia
A
0.700
GeneticVariation
CLINVAR
UBE2T, the Fanconi anemia core complex, and FANCD2 are recruited independently to chromatin: a basis for the regulation of FANCD2 monoubiquitination.
17938197
2007
rs750871999
VRK2;FANCL
Fanconi Anemia
A
0.700
GeneticVariation
CLINVAR
A novel ubiquitin ligase is deficient in Fanconi anemia.
12973351
2003