Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs10816595
rs10816595 		0.700 GeneticVariation GWASCAT Novel pleiotropic risk loci for melanoma and nevus density implicate multiple biological pathways. 30429480

2018
dbSNP: rs12696304
rs12696304 		G 0.700 GeneticVariation GWASCAT Genome-wide meta-analysis identifies five new susceptibility loci for cutaneous malignant melanoma. 26237428

2015
dbSNP: rs12696304
rs12696304 		0.700 GeneticVariation GWASCAT Novel pleiotropic risk loci for melanoma and nevus density implicate multiple biological pathways. 30429480

2018
dbSNP: rs2111398
rs2111398 		G 0.700 GeneticVariation GWASCAT Genome-wide meta-analysis identifies five new susceptibility loci for cutaneous malignant melanoma. 26237428

2015
dbSNP: rs2695237
rs2695237 		0.700 GeneticVariation GWASCAT Novel pleiotropic risk loci for melanoma and nevus density implicate multiple biological pathways. 30429480

2018
dbSNP: rs498136
rs498136 		0.700 GeneticVariation GWASCAT Novel pleiotropic risk loci for melanoma and nevus density implicate multiple biological pathways. 30429480

2018
dbSNP: rs498136
rs498136 		A 0.700 GeneticVariation GWASCAT Genome-wide meta-analysis identifies five new susceptibility loci for cutaneous malignant melanoma. 26237428

2015
dbSNP: rs7041168
rs7041168 		G 0.700 GeneticVariation GWASCAT Genome-wide meta-analysis identifies five new susceptibility loci for cutaneous malignant melanoma. 26237428

2015
dbSNP: rs75691080
rs75691080 		T 0.700 GeneticVariation GWASCAT Genome-wide meta-analysis identifies five new susceptibility loci for cutaneous malignant melanoma. 26237428

2015
dbSNP: rs12512631
rs12512631 		0.010 GeneticVariation BEFREE We found association between SNP rs12512631, located 3'downstream of GC, and risk of CM that seems to fit a dominant model (OR 1.63 95%CI 1.23-2.17 p-value 7×10(-4)). 23544077

2013
dbSNP: rs7855483
rs7855483 		0.010 GeneticVariation BEFREE In addition, three SNPs in the ACO1 gene, rs7855483 (P (trend) = 0.002), rs17288067 (P (trend) = 0.0009), and rs10813813 (P (trend) = 0.005), showed the strongest associations with CMM risk. 20574843

2010
dbSNP: rs10813813
rs10813813
ACO1
0.010 GeneticVariation BEFREE In addition, three SNPs in the ACO1 gene, rs7855483 (P (trend) = 0.002), rs17288067 (P (trend) = 0.0009), and rs10813813 (P (trend) = 0.005), showed the strongest associations with CMM risk. 20574843

2010
dbSNP: rs17288067
rs17288067
ACO1
0.010 GeneticVariation BEFREE In addition, three SNPs in the ACO1 gene, rs7855483 (P (trend) = 0.002), rs17288067 (P (trend) = 0.0009), and rs10813813 (P (trend) = 0.005), showed the strongest associations with CMM risk. 20574843

2010
dbSNP: rs1636744
rs1636744
AHR
0.700 GeneticVariation GWASCAT Novel pleiotropic risk loci for melanoma and nevus density implicate multiple biological pathways. 30429480

2018
dbSNP: rs1636744
rs1636744
AHR
T 0.700 GeneticVariation GWASCAT Genome-wide meta-analysis identifies five new susceptibility loci for cutaneous malignant melanoma. 26237428

2015
dbSNP: rs1057519786
rs1057519786
ARAF
G 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016
dbSNP: rs1057519786
rs1057519786
ARAF
T 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016
dbSNP: rs1057519876
rs1057519876
ARAF
G 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016
dbSNP: rs72704658
rs72704658
ARNT
0.700 GeneticVariation GWASCAT Novel pleiotropic risk loci for melanoma and nevus density implicate multiple biological pathways. 30429480

2018
dbSNP: rs73008229
rs73008229
ATM ; C11orf65
0.700 GeneticVariation GWASCAT Novel pleiotropic risk loci for melanoma and nevus density implicate multiple biological pathways. 30429480

2018
dbSNP: rs1023835002
rs1023835002
B2M ; PATL2
T 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016
dbSNP: rs1023835002
rs1023835002
B2M ; PATL2
G 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016
dbSNP: rs1057519877
rs1057519877
B2M ; PATL2
A 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016
dbSNP: rs1057519879
rs1057519879
B2M ; PATL2
C 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016
dbSNP: rs1057519879
rs1057519879
B2M ; PATL2
G 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016