Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs6911302
rs6911302
Entrez Id: 9750
Gene Symbol: RIPOR2
RIPOR2
CUI: C0200635
Disease:
Lymphocyte Count measurement 		C 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs186361153
rs186361153
Entrez Id: 9750
Gene Symbol: RIPOR2
RIPOR2
CUI: C3548479
Disease:
response to bronchodilator 		G 0.700 GeneticVariation GWASCAT A genome-wide association study identifies risk loci for spirometric measures among smokers of European and African ancestry. 26634245 2015
dbSNP: rs79014439
rs79014439
Entrez Id: 9750
Gene Symbol: RIPOR2
RIPOR2
CUI: C0004096
Disease:
Asthma 		G 0.700 GeneticVariation GWASCAT Genome-Wide Association Study Identifies Novel Loci Associated With Diisocyanate-Induced Occupational Asthma. 25918132 2015
dbSNP: rs12194442
rs12194442
Entrez Id: 9750
Gene Symbol: RIPOR2
RIPOR2
CUI: C4528257
Disease:
Corpuscular Hemoglobin Concentration Mean 		0.700 GeneticVariation GWASDB Seventy-five genetic loci influencing the human red blood cell. 23222517 2012
dbSNP: rs680009
rs680009
Entrez Id: 9750;105374981
Gene Symbol: RIPOR2;LOC105374981
RIPOR2;LOC105374981
CUI: C0003873
Disease:
Rheumatoid Arthritis 		0.700 GeneticVariation GWASDB REL, encoding a member of the NF-kappaB family of transcription factors, is a newly defined risk locus for rheumatoid arthritis. 19503088 2009
dbSNP: rs875989828
rs875989828
Entrez Id: 9750
Gene Symbol: RIPOR2
RIPOR2
CUI: C4225298
Disease:
DEAFNESS, AUTOSOMAL RECESSIVE 104 		T 0.700 CausalMutation CLINVAR
dbSNP: rs10946737
rs10946737
Entrez Id: 9750
Gene Symbol: RIPOR2
RIPOR2
CUI: C0860207
Disease:
Drug-Induced Liver Disease 		0.010 GeneticVariation BEFREE On the basis of this case-control study, SNP rs10946737 in FAM65B may be associated with susceptibility to ATDH in Chinese Han anti-TB treatment patients. 30720667 2019
dbSNP: rs9393597
rs9393597
Entrez Id: 9750
Gene Symbol: RIPOR2
RIPOR2
CUI: C0678222
Disease:
Breast Carcinoma 		0.010 GeneticVariation BEFREE In this replication analysis, rs9393597 was not associated with breast cancer risk for BRCA2 mutation carriers (HR = 1.09, 95 % CI 0.96-1.24, p = 0.18). 23011509 2012
dbSNP: rs9393597
rs9393597
Entrez Id: 9750
Gene Symbol: RIPOR2
RIPOR2
CUI: C0006142
Disease:
Malignant neoplasm of breast 		0.010 GeneticVariation BEFREE In this replication analysis, rs9393597 was not associated with breast cancer risk for BRCA2 mutation carriers (HR = 1.09, 95 % CI 0.96-1.24, p = 0.18). 23011509 2012