Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs12532102
rs12532102
Entrez Id: 55536
Gene Symbol: CDCA7L
CDCA7L
CUI: C1836230
Disease:
HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, SUSCEPTIBILITY TO 		A 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
dbSNP: rs12532102
rs12532102
Entrez Id: 55536
Gene Symbol: CDCA7L
CDCA7L
CUI: C1836233
Disease:
AIDS, PROGRESSION TO 		A 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
dbSNP: rs12532102
rs12532102
Entrez Id: 55536
Gene Symbol: CDCA7L
CDCA7L
CUI: C1836231
Disease:
HIV-1, RESISTANCE TO 		A 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
dbSNP: rs12532102
rs12532102
Entrez Id: 55536
Gene Symbol: CDCA7L
CDCA7L
CUI: C1836232
Disease:
ACQUIRED IMMUNODEFICIENCY SYNDROME, PROGRESSION TO 		A 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
dbSNP: rs12532102
rs12532102
Entrez Id: 55536
Gene Symbol: CDCA7L
CDCA7L
CUI: C0376705
Disease:
Viral Load result 		A 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
dbSNP: rs7971
rs7971
Entrez Id: 8701;55536
Gene Symbol: DNAH11;CDCA7L
DNAH11;CDCA7L
CUI: C0678222
Disease:
Breast Carcinoma 		A 0.700 GeneticVariation GWASCAT Association analysis identifies 65 new breast cancer risk loci. 29059683 2017
dbSNP: rs1128226
rs1128226
Entrez Id: 8701;55536
Gene Symbol: DNAH11;CDCA7L
DNAH11;CDCA7L
CUI: C0026764
Disease:
Multiple Myeloma 		A 0.700 GeneticVariation GWASDB Common variation at 3q26.2, 6p21.33, 17p11.2 and 22q13.1 influences multiple myeloma risk. 23955597 2013
dbSNP: rs12234262
rs12234262
Entrez Id: 55536
Gene Symbol: CDCA7L
CDCA7L
CUI: C0026764
Disease:
Multiple Myeloma 		A 0.700 GeneticVariation GWASDB Common variation at 3q26.2, 6p21.33, 17p11.2 and 22q13.1 influences multiple myeloma risk. 23955597 2013
dbSNP: rs4445125
rs4445125
Entrez Id: 55536
Gene Symbol: CDCA7L
CDCA7L
CUI: C0026764
Disease:
Multiple Myeloma 		A 0.700 GeneticVariation GWASDB Common variation at 3q26.2, 6p21.33, 17p11.2 and 22q13.1 influences multiple myeloma risk. 23955597 2013
dbSNP: rs7971
rs7971
Entrez Id: 8701;55536
Gene Symbol: DNAH11;CDCA7L
DNAH11;CDCA7L
CUI: C0026764
Disease:
Multiple Myeloma 		A 0.700 GeneticVariation GWASDB Common variation at 3q26.2, 6p21.33, 17p11.2 and 22q13.1 influences multiple myeloma risk. 23955597 2013
dbSNP: rs1128226
rs1128226
Entrez Id: 8701;55536
Gene Symbol: DNAH11;CDCA7L
DNAH11;CDCA7L
CUI: C0026764
Disease:
Multiple Myeloma 		0.700 GeneticVariation GWASDB Common variation at 3p22.1 and 7p15.3 influences multiple myeloma risk. 22120009 2011
dbSNP: rs12234262
rs12234262
Entrez Id: 55536
Gene Symbol: CDCA7L
CDCA7L
CUI: C0026764
Disease:
Multiple Myeloma 		0.700 GeneticVariation GWASDB Common variation at 3p22.1 and 7p15.3 influences multiple myeloma risk. 22120009 2011
dbSNP: rs12540021
rs12540021
Entrez Id: 55536
Gene Symbol: CDCA7L
CDCA7L
CUI: C0026764
Disease:
Multiple Myeloma 		0.700 GeneticVariation GWASDB Common variation at 3p22.1 and 7p15.3 influences multiple myeloma risk. 22120009 2011
dbSNP: rs12700325
rs12700325
Entrez Id: 8701;55536
Gene Symbol: DNAH11;CDCA7L
DNAH11;CDCA7L
CUI: C0026764
Disease:
Multiple Myeloma 		0.700 GeneticVariation GWASDB Common variation at 3p22.1 and 7p15.3 influences multiple myeloma risk. 22120009 2011
dbSNP: rs4534048
rs4534048
Entrez Id: 55536
Gene Symbol: CDCA7L
CDCA7L
CUI: C0026764
Disease:
Multiple Myeloma 		0.700 GeneticVariation GWASDB Common variation at 3p22.1 and 7p15.3 influences multiple myeloma risk. 22120009 2011
dbSNP: rs56249828
rs56249828
Entrez Id: 55536
Gene Symbol: CDCA7L
CDCA7L
CUI: C0026764
Disease:
Multiple Myeloma 		0.700 GeneticVariation GWASDB Common variation at 3p22.1 and 7p15.3 influences multiple myeloma risk. 22120009 2011
dbSNP: rs56268505
rs56268505
Entrez Id: 8701;55536
Gene Symbol: DNAH11;CDCA7L
DNAH11;CDCA7L
CUI: C0026764
Disease:
Multiple Myeloma 		0.700 GeneticVariation GWASDB Common variation at 3p22.1 and 7p15.3 influences multiple myeloma risk. 22120009 2011
dbSNP: rs6976370
rs6976370
Entrez Id: 55536
Gene Symbol: CDCA7L
CDCA7L
CUI: C0026764
Disease:
Multiple Myeloma 		0.700 GeneticVariation GWASDB Common variation at 3p22.1 and 7p15.3 influences multiple myeloma risk. 22120009 2011
dbSNP: rs7971
rs7971
Entrez Id: 8701;55536
Gene Symbol: DNAH11;CDCA7L
DNAH11;CDCA7L
CUI: C0026764
Disease:
Multiple Myeloma 		0.700 GeneticVariation GWASDB Common variation at 3p22.1 and 7p15.3 influences multiple myeloma risk. 22120009 2011
dbSNP: rs1212535211
rs1212535211
Entrez Id: 8701;55536
Gene Symbol: DNAH11;CDCA7L
DNAH11;CDCA7L
CUI: C0008780
Disease:
Ciliary Motility Disorders 		T 0.700 GeneticVariation CLINVAR
dbSNP: rs1261703349
rs1261703349
Entrez Id: 8701;55536
Gene Symbol: DNAH11;CDCA7L
DNAH11;CDCA7L
CUI: C0008780
Disease:
Ciliary Motility Disorders 		T 0.700 CausalMutation CLINVAR
dbSNP: rs1554294478
rs1554294478
Entrez Id: 8701;55536
Gene Symbol: DNAH11;CDCA7L
DNAH11;CDCA7L
CUI: C2678473
Disease:
CILIARY DYSKINESIA, PRIMARY, 7 (disorder) 		G 0.700 CausalMutation CLINVAR
dbSNP: rs1554294478
rs1554294478
Entrez Id: 8701;55536
Gene Symbol: DNAH11;CDCA7L
DNAH11;CDCA7L
CUI: C0008780
Disease:
Ciliary Motility Disorders 		G 0.700 CausalMutation CLINVAR
dbSNP: rs551275210
rs551275210
Entrez Id: 8701;55536
Gene Symbol: DNAH11;CDCA7L
DNAH11;CDCA7L
CUI: C0008780
Disease:
Ciliary Motility Disorders 		T 0.700 CausalMutation CLINVAR