Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs9510787
rs9510787
Entrez Id: 55504
Gene Symbol: TNFRSF19
TNFRSF19
CUI: C2931822
Disease:
Nasopharyngeal carcinoma 		0.730 GeneticVariation BEFREE Conclusion Our systematic review identified 5 SNPs located on chromosome 6 ( rs2076483, rs2975042, rs3129055, rs9258122, and rs29232) and 1 ( rs9510787) on chromosome 13 as significantly associated with an increased risk of NPC in Chinese. 30126334 2018
dbSNP: rs9510787
rs9510787
Entrez Id: 55504
Gene Symbol: TNFRSF19
TNFRSF19
CUI: C2931822
Disease:
Nasopharyngeal carcinoma 		0.730 GeneticVariation BEFREE In this study, in southern China, where NPC is endemic, a single nucleotide polymorphism (SNP) in the EBV-encoded <i>RPMS1</i> gene (locus 155391: G > A [G155391A]) and seven host SNPs (rs1412829, rs28421666, rs2860580, rs2894207, rs31489, rs6774494, and rs9510787) were confirmed to be significantly associated with NPC risk in 50 NPC cases versus 54 hospital-based controls with throat washing specimens and 1925 NPC cases versus 1947 hospital-based controls with buffy coat samples, respectively. 29221111 2017
dbSNP: rs9510787
rs9510787
Entrez Id: 55504
Gene Symbol: TNFRSF19
TNFRSF19
CUI: C2931822
Disease:
Nasopharyngeal carcinoma 		0.730 GeneticVariation BEFREE Our results also provide support for associations reported from published NPC GWAS-rs6774494 (P = 1.5 × 10(-12); located in the MECOM gene region), rs9510787 (P = 5.0 × 10(-10); located in the TNFRSF19 gene region), and rs1412829/rs4977756/rs1063192 (P = 2.8 × 10(-8), P = 7.0 × 10(-7), and P = 8.4 × 10(-7), respectively; located in the CDKN2A/B gene region). 26545403 2016
dbSNP: rs9510787
rs9510787
Entrez Id: 55504
Gene Symbol: TNFRSF19
TNFRSF19
CUI: C2931822
Disease:
Nasopharyngeal carcinoma 		G 0.730 GeneticVariation GWASDB A genome-wide association study of nasopharyngeal carcinoma identifies three new susceptibility loci. 20512145 2010
dbSNP: rs11841272
rs11841272
Entrez Id: 55504
Gene Symbol: TNFRSF19
TNFRSF19
CUI: C0005938
Disease:
Bone Density 		T 0.700 GeneticVariation GWASCAT Joint Association Analysis Identified 18 New Loci for Bone Mineral Density. 30690781 2019
dbSNP: rs3814787
rs3814787
Entrez Id: 55504
Gene Symbol: TNFRSF19
TNFRSF19
CUI: C2985280
Disease:
Blood Protein Measurement 		G 0.700 GeneticVariation GWASCAT Co-regulatory networks of human serum proteins link genetics to disease. 30072576 2018
dbSNP: rs9510787
rs9510787
Entrez Id: 55504
Gene Symbol: TNFRSF19
TNFRSF19
CUI: C0027439
Disease:
Nasopharyngeal Neoplasms 		0.700 GeneticVariation GWASCAT A GWAS Meta-analysis and Replication Study Identifies a Novel Locus within CLPTM1L/TERT Associated with Nasopharyngeal Carcinoma in Individuals of Chinese Ancestry. 26545403 2016
dbSNP: rs9510787
rs9510787
Entrez Id: 55504
Gene Symbol: TNFRSF19
TNFRSF19
CUI: C0027439
Disease:
Nasopharyngeal Neoplasms 		G 0.700 GeneticVariation GWASCAT A genome-wide association study of nasopharyngeal carcinoma identifies three new susceptibility loci. 20512145 2010