Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2244012
rs2244012
Entrez Id: 10111
Gene Symbol: RAD50
RAD50
CUI: C0004096
Disease:
Asthma 		0.820 GeneticVariation BEFREE We conducted an association study by genotyping four SNPs (rs2244012 and rs6871536 in RAD50 as well as rs1295686 and rs1800925 in IL13) in 652 asthmatic children and age-matched 752 healthy controls from Northeastern Han Chinese to evaluate the asthma susceptibility with each individual SNP using SNaPshot genotyping method. 26365633 2016
dbSNP: rs2244012
rs2244012
Entrez Id: 10111
Gene Symbol: RAD50
RAD50
CUI: C0004096
Disease:
Asthma 		0.820 GeneticVariation GWASCAT Detection and interpretation of shared genetic influences on 42 human traits. 27182965 2016
dbSNP: rs2244012
rs2244012
Entrez Id: 10111
Gene Symbol: RAD50
RAD50
CUI: C0004096
Disease:
Asthma 		C 0.820 GeneticVariation GWASDB Multiple SNPs in the RAD50-IL13 region on chromosome 5q31.1 were associated with asthma: rs2244012 in intron 2 of RAD50 (P = 3.04E-07). 20159242 2010
dbSNP: rs2244012
rs2244012
Entrez Id: 10111
Gene Symbol: RAD50
RAD50
CUI: C0004096
Disease:
Asthma 		0.820 GeneticVariation BEFREE Multiple SNPs in the RAD50-IL13 region on chromosome 5q31.1 were associated with asthma: rs2244012 in intron 2 of RAD50 (P = 3.04E-07). 20159242 2010
dbSNP: rs2244012
rs2244012
Entrez Id: 10111
Gene Symbol: RAD50
RAD50
CUI: C0004096
Disease:
Asthma 		C 0.820 GeneticVariation GWASCAT Multiple SNPs in the RAD50-IL13 region on chromosome 5q31.1 were associated with asthma: rs2244012 in intron 2 of RAD50 (P = 3.04E-07). 20159242 2010
dbSNP: rs6871536
rs6871536
Entrez Id: 10111;101927761
Gene Symbol: RAD50;TH2LCRR
RAD50;TH2LCRR
CUI: C0004096
Disease:
Asthma 		0.710 GeneticVariation BEFREE We conducted an association study by genotyping four SNPs (rs2244012 and rs6871536 in RAD50 as well as rs1295686 and rs1800925 in IL13) in 652 asthmatic children and age-matched 752 healthy controls from Northeastern Han Chinese to evaluate the asthma susceptibility with each individual SNP using SNaPshot genotyping method. 26365633 2016
dbSNP: rs6871536
rs6871536
Entrez Id: 10111;101927761
Gene Symbol: RAD50;TH2LCRR
RAD50;TH2LCRR
CUI: C0004096
Disease:
Asthma 		0.710 GeneticVariation GWASDB Identification of IL6R and chromosome 11q13.5 as risk loci for asthma. 21907864 2011
dbSNP: rs6871536
rs6871536
Entrez Id: 10111;101927761
Gene Symbol: RAD50;TH2LCRR
RAD50;TH2LCRR
CUI: C0004096
Disease:
Asthma 		0.710 GeneticVariation GWASDB Genome-wide association study of asthma identifies RAD50-IL13 and HLA-DR/DQ regions. 20159242 2010
dbSNP: rs6871536
rs6871536
Entrez Id: 10111;101927761
Gene Symbol: RAD50;TH2LCRR
RAD50;TH2LCRR
CUI: C0004096
Disease:
Asthma 		0.710 GeneticVariation GWASDB A large-scale, consortium-based genomewide association study of asthma. 20860503 2010
dbSNP: rs2299012
rs2299012
Entrez Id: 10111
Gene Symbol: RAD50
RAD50
CUI: C0264408
Disease:
Childhood asthma 		0.700 GeneticVariation GWASCAT Genetic Architectures of Childhood- and Adult-Onset Asthma Are Partly Distinct. 30929738 2019
dbSNP: rs2299012
rs2299012
Entrez Id: 10111
Gene Symbol: RAD50
RAD50
CUI: C0004096
Disease:
Asthma 		C 0.700 GeneticVariation GWASCAT Genetic Architectures of Childhood- and Adult-Onset Asthma Are Partly Distinct. 30929738 2019
dbSNP: rs75765453
rs75765453
Entrez Id: 10111
Gene Symbol: RAD50
RAD50
CUI: C0200638
Disease:
Eosinophil count procedure 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs2706362
rs2706362
Entrez Id: 10111
Gene Symbol: RAD50
RAD50
CUI: C0004096
Disease:
Asthma 		0.700 GeneticVariation GWASCAT A genome-wide cross-trait analysis from UK Biobank highlights the shared genetic architecture of asthma and allergic diseases. 29785011 2018
dbSNP: rs9687749
rs9687749
Entrez Id: 10111
Gene Symbol: RAD50
RAD50
CUI: C2607914
Disease:
Allergic rhinitis (disorder) 		T 0.700 GeneticVariation GWASCAT Genome-wide association and HLA fine-mapping studies identify risk loci and genetic pathways underlying allergic rhinitis. 30013184 2018
dbSNP: rs121912628
rs121912628
Entrez Id: 10111
Gene Symbol: RAD50
RAD50
CUI: C2751318
Disease:
Nijmegen Breakage Syndrome-Like Disorder 		T 0.700 GeneticVariation CLINVAR The germline variants in DNA repair genes in pediatric medulloblastoma: a challenge for current therapeutic strategies. 28376765 2017
dbSNP: rs2040704
rs2040704
Entrez Id: 10111;101927761
Gene Symbol: RAD50;TH2LCRR
RAD50;TH2LCRR
CUI: C0004096
Disease:
Asthma 		0.700 GeneticVariation GWASCAT Identification of Four Novel Loci in Asthma in European American and African American Populations. 27611488 2017
dbSNP: rs778555849
rs778555849
Entrez Id: 10111;101927761
Gene Symbol: RAD50;TH2LCRR
RAD50;TH2LCRR
CUI: C0027672
Disease:
Neoplastic Syndromes, Hereditary 		T 0.700 CausalMutation CLINVAR The frequency of cancer predisposition gene mutations in hereditary breast and ovarian cancer patients in Taiwan: From BRCA1/2 to multi-gene panels. 28961279 2017
dbSNP: rs786201897
rs786201897
Entrez Id: 10111
Gene Symbol: RAD50
RAD50
CUI: C0027672
Disease:
Neoplastic Syndromes, Hereditary 		TA 0.700 CausalMutation CLINVAR Almost 2% of Spanish breast cancer families are associated to germline pathogenic mutations in the ATM gene. 27913932 2017
dbSNP: rs1060501941
rs1060501941
Entrez Id: 10111
Gene Symbol: RAD50
RAD50
CUI: C2751318
Disease:
Nijmegen Breakage Syndrome-Like Disorder 		T 0.700 GeneticVariation CLINVAR Panel Testing for Familial Breast Cancer: Calibrating the Tension Between Research and Clinical Care. 26786923 2016
dbSNP: rs1247689593
rs1247689593
Entrez Id: 10111
Gene Symbol: RAD50
RAD50
CUI: C0027672
Disease:
Neoplastic Syndromes, Hereditary 		T 0.700 CausalMutation CLINVAR Hereditary truncating mutations of DNA repair and other genes in BRCA1/BRCA2/PALB2-negatively tested breast cancer patients. 26822949 2016
dbSNP: rs1247689593
rs1247689593
Entrez Id: 10111
Gene Symbol: RAD50
RAD50
CUI: C2751318
Disease:
Nijmegen Breakage Syndrome-Like Disorder 		T 0.700 GeneticVariation CLINVAR Hereditary truncating mutations of DNA repair and other genes in BRCA1/BRCA2/PALB2-negatively tested breast cancer patients. 26822949 2016
dbSNP: rs149201802
rs149201802
Entrez Id: 10111
Gene Symbol: RAD50
RAD50
CUI: C0027672
Disease:
Neoplastic Syndromes, Hereditary 		G 0.700 CausalMutation CLINVAR Multigene testing of moderate-risk genes: be mindful of the missense. 26787654 2016
dbSNP: rs1554098706
rs1554098706
Entrez Id: 10111
Gene Symbol: RAD50
RAD50
CUI: C0027672
Disease:
Neoplastic Syndromes, Hereditary 		CT 0.700 CausalMutation CLINVAR Multiple gene sequencing for risk assessment in patients with early-onset or familial breast cancer. 26824983 2016
dbSNP: rs2706345
rs2706345
Entrez Id: 10111
Gene Symbol: RAD50
RAD50
CUI: C0200641
Disease:
Blood basophil count (lab test) 		A 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs2706345
rs2706345
Entrez Id: 10111
Gene Symbol: RAD50
RAD50
CUI: C0200638
Disease:
Eosinophil count procedure 		A 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016