CBX7, chromobox 7, 23492

N. diseases: 73; N. variants: 11
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs877529
rs877529
Entrez Id: 23492
Gene Symbol: CBX7
CBX7
CUI: C0026764
Disease:
Multiple Myeloma 		0.810 GeneticVariation BEFREE Common single-nucleotide polymorphisms (SNPs) at 2p23.3 (rs6746082), 3p22.1 (rs1052501), 3q26.2 (rs10936599), 6p21.33 (rs2285803), 7p15.3 (rs4487645), 17p11.2 (rs4273077), and 22q13.1 (rs877529) have recently been shown to influence MM risk. 24449210 2014
dbSNP: rs877529
rs877529
Entrez Id: 23492
Gene Symbol: CBX7
CBX7
CUI: C0026764
Disease:
Multiple Myeloma 		A 0.810 GeneticVariation GWASDB Common variation at 3q26.2, 6p21.33, 17p11.2 and 22q13.1 influences multiple myeloma risk. 23955597 2013
dbSNP: rs877529
rs877529
Entrez Id: 23492
Gene Symbol: CBX7
CBX7
CUI: C0026764
Disease:
Multiple Myeloma 		A 0.810 GeneticVariation GWASCAT Common variation at 3q26.2, 6p21.33, 17p11.2 and 22q13.1 influences multiple myeloma risk. 23955597 2013
dbSNP: rs139371
rs139371
Entrez Id: 23492
Gene Symbol: CBX7
CBX7
CUI: C0026764
Disease:
Multiple Myeloma 		G 0.800 GeneticVariation GWASDB Common variation at 3q26.2, 6p21.33, 17p11.2 and 22q13.1 influences multiple myeloma risk. 23955597 2013
dbSNP: rs139371
rs139371
Entrez Id: 23492
Gene Symbol: CBX7
CBX7
CUI: C0026764
Disease:
Multiple Myeloma 		A 0.800 GeneticVariation GWASCAT The CCND1 c.870G>A polymorphism is a risk factor for t(11;14)(q13;q32) multiple myeloma. 23502783 2013
dbSNP: rs139380
rs139380
Entrez Id: 23492
Gene Symbol: CBX7
CBX7
CUI: C0014772
Disease:
Red Blood Cell Count measurement 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs1005300
rs1005300
Entrez Id: 23492
Gene Symbol: CBX7
CBX7
CUI: C0268381
Disease:
Primary amyloidosis 		G 0.700 GeneticVariation GWASCAT Genome-wide association study of immunoglobulin light chain amyloidosis in three patient cohorts: comparison with myeloma. 28025584 2017
dbSNP: rs139402
rs139402
Entrez Id: 23492
Gene Symbol: CBX7
CBX7
CUI: C0026764
Disease:
Multiple Myeloma 		C 0.700 GeneticVariation GWASCAT Genome-wide association study identifies multiple susceptibility loci for multiple myeloma. 27363682 2016
dbSNP: rs713909
rs713909
Entrez Id: 23492
Gene Symbol: CBX7
CBX7
CUI: C0023508
Disease:
White Blood Cell Count procedure 		C 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs713909
rs713909
Entrez Id: 23492
Gene Symbol: CBX7
CBX7
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: rs12158877
rs12158877
Entrez Id: 23492
Gene Symbol: CBX7
CBX7
CUI: C0026764
Disease:
Multiple Myeloma 		C 0.700 GeneticVariation GWASDB Common variation at 3q26.2, 6p21.33, 17p11.2 and 22q13.1 influences multiple myeloma risk. 23955597 2013
dbSNP: rs139385
rs139385
Entrez Id: 23492
Gene Symbol: CBX7
CBX7
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: rs710190
rs710190
Entrez Id: 23492
Gene Symbol: CBX7
CBX7
CUI: C0026764
Disease:
Multiple Myeloma 		G 0.700 GeneticVariation GWASDB Common variation at 3q26.2, 6p21.33, 17p11.2 and 22q13.1 influences multiple myeloma risk. 23955597 2013
dbSNP: rs713841
rs713841
Entrez Id: 23492
Gene Symbol: CBX7
CBX7
CUI: C0026764
Disease:
Multiple Myeloma 		G 0.700 GeneticVariation GWASDB Common variation at 3q26.2, 6p21.33, 17p11.2 and 22q13.1 influences multiple myeloma risk. 23955597 2013
dbSNP: rs139394
rs139394
Entrez Id: 23492
Gene Symbol: CBX7
CBX7
CUI: C2239176
Disease:
Liver carcinoma 		0.010 GeneticVariation BEFREE Our findings suggest that <i>CBX4</i> rs2289728 and <i>CBX7</i> rs139394 are protective SNPs against HCC. 31211140 2019
dbSNP: rs710190
rs710190
Entrez Id: 23492
Gene Symbol: CBX7
CBX7
CUI: C2239176
Disease:
Liver carcinoma 		0.010 GeneticVariation BEFREE Interaction between rs2036316 and HBsAg increased the risk of HCC (<i>P</i> = 0.02, OR = 6.88, 95% CI: 5.20-9.11), whereas SNP-SNP interaction between rs710190 and rs139394 reduced the risk of HCC (<i>P</i> = 0.03, OR = 0.33, 95% CI: 0.12-0.91). 31211140 2019