Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1063192
rs1063192
CDKN2B ; CDKN2B-AS1
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: rs1412829
rs1412829
CDKN2B-AS1
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: rs1412829
rs1412829
CDKN2B-AS1
0.700 GeneticVariation GWASCAT A genome-wide association study of nasopharyngeal carcinoma identifies three new susceptibility loci. 20512145

2010
dbSNP: rs1572072
rs1572072 		0.700 GeneticVariation GWASCAT A genome-wide association study of nasopharyngeal carcinoma identifies three new susceptibility loci. 20512145

2010
dbSNP: rs28421666
rs28421666 		0.700 GeneticVariation GWASCAT An extended genome-wide association study identifies novel susceptibility loci for nasopharyngeal carcinoma. 27436580

2016
dbSNP: rs28421666
rs28421666 		0.700 GeneticVariation GWASCAT A genome-wide association study of nasopharyngeal carcinoma identifies three new susceptibility loci. 20512145

2010
dbSNP: rs2860580
rs2860580
HLA-A
0.700 GeneticVariation GWASCAT A genome-wide association study of nasopharyngeal carcinoma identifies three new susceptibility loci. 20512145

2010
dbSNP: rs2860580
rs2860580
HLA-A
0.700 GeneticVariation GWASCAT An extended genome-wide association study identifies novel susceptibility loci for nasopharyngeal carcinoma. 27436580

2016
dbSNP: rs2894207
rs2894207
HLA-B ; LINC02571
0.700 GeneticVariation GWASCAT An extended genome-wide association study identifies novel susceptibility loci for nasopharyngeal carcinoma. 27436580

2016
dbSNP: rs2894207
rs2894207
HLA-B ; LINC02571
0.700 GeneticVariation GWASCAT A genome-wide association study of nasopharyngeal carcinoma identifies three new susceptibility loci. 20512145

2010
dbSNP: rs31489
rs31489
CLPTM1L
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: rs3731239
rs3731239
CDKN2A
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: rs401681
rs401681
CLPTM1L
0.700 GeneticVariation GWASCAT An extended genome-wide association study identifies novel susceptibility loci for nasopharyngeal carcinoma. 27436580

2016
dbSNP: rs4977756
rs4977756
CDKN2B-AS1
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: rs6498114
rs6498114
CIITA ; LOC105371080
0.700 GeneticVariation GWASCAT An extended genome-wide association study identifies novel susceptibility loci for nasopharyngeal carcinoma. 27436580

2016
dbSNP: rs6774494
rs6774494
MECOM
0.700 GeneticVariation GWASCAT A genome-wide association study of nasopharyngeal carcinoma identifies three new susceptibility loci. 20512145

2010
dbSNP: rs6774494
rs6774494
MECOM
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
TNFRSF19
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: rs104886003
rs104886003
PIK3CA
A 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016
dbSNP: rs104894229
rs104894229
HRAS ; LRRC56
A 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016
dbSNP: rs11554290
rs11554290
NRAS
A 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016
dbSNP: rs121913255
rs121913255
NRAS
A 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016
dbSNP: rs138729528
rs138729528
TP53
A 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016
dbSNP: rs162171
rs162171
CEP128
A 0.700 GeneticVariation GWASCAT Genome-Wide Association Study of Susceptibility Loci for Radiation-Induced Brain Injury. 30299488

2019
dbSNP: rs180177133
rs180177133
PALB2
A 0.700 CausalMutation CLINVAR