Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1042522
rs1042522
CUI: C0007134
Disease: Renal Cell Carcinoma
Renal Cell Carcinoma
0.020 GeneticVariation BEFREE Taken together, this is the first study to show that a variant genotype of p53 Arg(72)Pro or MDM2 SNP309 may modify the arsenic-related RCC risk even in a non-obvious arsenic exposure area. 21982800

2011

dbSNP: rs1042522
rs1042522
CUI: C0007134
Disease: Renal Cell Carcinoma
Renal Cell Carcinoma
0.020 GeneticVariation BEFREE Polymorphisms of p53 Arg(72)Pro and p21 Ser(31)Arg did not show significant association with RCC. 17634539

2007

dbSNP: rs1057519977
rs1057519977
CUI: C0007134
Disease: Renal Cell Carcinoma
Renal Cell Carcinoma
C 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016

dbSNP: rs1057519978
rs1057519978
CUI: C0007134
Disease: Renal Cell Carcinoma
Renal Cell Carcinoma
G 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016

dbSNP: rs1057519978
rs1057519978
CUI: C0007134
Disease: Renal Cell Carcinoma
Renal Cell Carcinoma
T 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016

dbSNP: rs1057519978
rs1057519978
CUI: C0007134
Disease: Renal Cell Carcinoma
Renal Cell Carcinoma
C 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016

dbSNP: rs1057519983
rs1057519983
CUI: C0007134
Disease: Renal Cell Carcinoma
Renal Cell Carcinoma
G 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016

dbSNP: rs1057519992
rs1057519992
CUI: C0007134
Disease: Renal Cell Carcinoma
Renal Cell Carcinoma
A 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016

dbSNP: rs1057519992
rs1057519992
CUI: C0007134
Disease: Renal Cell Carcinoma
Renal Cell Carcinoma
C 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016

dbSNP: rs1057519999
rs1057519999
CUI: C0007134
Disease: Renal Cell Carcinoma
Renal Cell Carcinoma
C 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016

dbSNP: rs1057520001
rs1057520001
CUI: C0007134
Disease: Renal Cell Carcinoma
Renal Cell Carcinoma
0.010 GeneticVariation BEFREE Polymorphisms of p53 Arg(72)Pro and p21 Ser(31)Arg did not show significant association with RCC. 17634539

2007

dbSNP: rs1057520002
rs1057520002
CUI: C0007134
Disease: Renal Cell Carcinoma
Renal Cell Carcinoma
C 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016

dbSNP: rs1057520002
rs1057520002
CUI: C0007134
Disease: Renal Cell Carcinoma
Renal Cell Carcinoma
G 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016

dbSNP: rs1057520003
rs1057520003
CUI: C0007134
Disease: Renal Cell Carcinoma
Renal Cell Carcinoma
G 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016

dbSNP: rs1057520007
rs1057520007
CUI: C0007134
Disease: Renal Cell Carcinoma
Renal Cell Carcinoma
A 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016

dbSNP: rs1057520007
rs1057520007
CUI: C0007134
Disease: Renal Cell Carcinoma
Renal Cell Carcinoma
C 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016

dbSNP: rs1057520007
rs1057520007
CUI: C0007134
Disease: Renal Cell Carcinoma
Renal Cell Carcinoma
G 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016

dbSNP: rs1131691014
rs1131691014
CUI: C0007134
Disease: Renal Cell Carcinoma
Renal Cell Carcinoma
0.020 GeneticVariation BEFREE Taken together, this is the first study to show that a variant genotype of p53 Arg(72)Pro or MDM2 SNP309 may modify the arsenic-related RCC risk even in a non-obvious arsenic exposure area. 21982800

2011

dbSNP: rs1131691014
rs1131691014
CUI: C0007134
Disease: Renal Cell Carcinoma
Renal Cell Carcinoma
0.020 GeneticVariation BEFREE Polymorphisms of p53 Arg(72)Pro and p21 Ser(31)Arg did not show significant association with RCC. 17634539

2007

dbSNP: rs121912657
rs121912657
CUI: C0007134
Disease: Renal Cell Carcinoma
Renal Cell Carcinoma
A 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016

dbSNP: rs121912666
rs121912666
CUI: C0007134
Disease: Renal Cell Carcinoma
Renal Cell Carcinoma
C 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016

dbSNP: rs121912666
rs121912666
CUI: C0007134
Disease: Renal Cell Carcinoma
Renal Cell Carcinoma
G 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016

dbSNP: rs28934573
rs28934573
CUI: C0007134
Disease: Renal Cell Carcinoma
Renal Cell Carcinoma
A 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016

dbSNP: rs28934573
rs28934573
CUI: C0007134
Disease: Renal Cell Carcinoma
Renal Cell Carcinoma
T 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016

dbSNP: rs28934573
rs28934573
CUI: C0007134
Disease: Renal Cell Carcinoma
Renal Cell Carcinoma
C 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016