Source: ALL

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 7299
Gene Symbol: TYR
TYR
CUI: C0025202
Disease: melanoma
melanoma 		0.500 GeneticVariation GWASDB Identification of a melanoma susceptibility locus and somatic mutation in TET2. 24980573

2014
Entrez Id: 4507
Gene Symbol: MTAP
MTAP
CUI: C0025202
Disease: melanoma
melanoma 		0.500 GeneticVariation GWASDB A unique genome-wide association analysis in extended Utah high-risk pedigrees identifies a novel melanoma risk variant on chromosome arm 10q. 21706340

2012
Entrez Id: 142
Gene Symbol: PARP1
PARP1
CUI: C0025202
Disease: melanoma
melanoma 		0.500 GeneticVariation GWASDB Genome-wide association study identifies a new melanoma susceptibility locus at 1q21.3. 21983785

2011
Entrez Id: 51151
Gene Symbol: SLC45A2
SLC45A2
CUI: C0025202
Disease: melanoma
melanoma 		0.500 GeneticVariation GWASDB Genome-wide association study identifies three new melanoma susceptibility loci. 21983787

2011
Entrez Id: 472
Gene Symbol: ATM
ATM
CUI: C0025202
Disease: melanoma
melanoma 		0.500 GeneticVariation GWASDB Genome-wide association study identifies three new melanoma susceptibility loci. 21983787

2011
Entrez Id: 7299
Gene Symbol: TYR
TYR
CUI: C0025202
Disease: melanoma
melanoma 		0.500 GeneticVariation GWASDB A unique genome-wide association analysis in extended Utah high-risk pedigrees identifies a novel melanoma risk variant on chromosome arm 10q. 21706340

2012
Entrez Id: 7299
Gene Symbol: TYR
TYR
CUI: C0025202
Disease: melanoma
melanoma 		0.500 GeneticVariation GWASDB Genome-wide association study identifies three new melanoma susceptibility loci. 21983787

2011
Entrez Id: 4507
Gene Symbol: MTAP
MTAP
CUI: C0025202
Disease: melanoma
melanoma 		0.500 GeneticVariation GWASDB Genome-wide association study identifies three loci associated with melanoma risk. 19578364

2009
Entrez Id: 7299
Gene Symbol: TYR
TYR
CUI: C0025202
Disease: melanoma
melanoma 		0.500 GeneticVariation GWASDB MC1R and TYR are associated with pigmentation, freckling and cutaneous sun sensitivity, well-recognized melanoma risk factors. 19578364

2009
Entrez Id: 4507
Gene Symbol: MTAP
MTAP
CUI: C0025202
Disease: melanoma
melanoma 		0.500 GeneticVariation GWASDB Genome-wide association study identifies three new melanoma susceptibility loci. 21983787

2011
Entrez Id: 841
Gene Symbol: CASP8
CASP8
CUI: C0025202
Disease: melanoma
melanoma 		0.470 GeneticVariation GWASDB Genome-wide association study identifies three new melanoma susceptibility loci. 21983787

2011
Entrez Id: 79068
Gene Symbol: FTO
FTO
CUI: C0025202
Disease: melanoma
melanoma 		0.440 GeneticVariation GWASDB In addition to identifying a new melanoma-susceptibility locus, this is to our knowledge the first study to identify and replicate an association with SNPs in FTO not related to body mass index (BMI). 23455637

2013
Entrez Id: 4600
Gene Symbol: MX2
MX2
CUI: C0025202
Disease: melanoma
melanoma 		0.410 GeneticVariation GWASDB Genome-wide association study identifies three new melanoma susceptibility loci. 21983787

2011
Entrez Id: 8398
Gene Symbol: PLA2G6
PLA2G6
CUI: C0025202
Disease: melanoma
melanoma 		0.170 GeneticVariation GWASDB A unique genome-wide association analysis in extended Utah high-risk pedigrees identifies a novel melanoma risk variant on chromosome arm 10q. 21706340

2012
Entrez Id: 8398
Gene Symbol: PLA2G6
PLA2G6
CUI: C0025202
Disease: melanoma
melanoma 		0.170 GeneticVariation GWASDB Genome-wide association study identifies three loci associated with melanoma risk. 19578364

2009
Entrez Id: 81037
Gene Symbol: CLPTM1L
CLPTM1L
CUI: C0025202
Disease: melanoma
melanoma 		0.160 GeneticVariation GWASDB Genome-wide association study identifies three new melanoma susceptibility loci. 21983787

2011
Entrez Id: 54790
Gene Symbol: TET2
TET2
CUI: C0025202
Disease: melanoma
melanoma 		0.150 GeneticVariation GWASDB Identification of a melanoma susceptibility locus and somatic mutation in TET2. 24980573

2014
Entrez Id: 8924
Gene Symbol: HERC2
HERC2
CUI: C0025202
Disease: melanoma
melanoma 		0.120 GeneticVariation GWASDB Genome-wide association study identifies novel loci predisposing to cutaneous melanoma. 21926416

2011
Entrez Id: 23054
Gene Symbol: NCOA6
NCOA6
CUI: C0025202
Disease: melanoma
melanoma 		0.120 GeneticVariation GWASDB Common sequence variants on 20q11.22 confer melanoma susceptibility. 18488026

2008
Entrez Id: 51654
Gene Symbol: CDK5RAP1
CDK5RAP1
CUI: C0025202
Disease: melanoma
melanoma 		0.110 GeneticVariation GWASDB Common sequence variants on 20q11.22 confer melanoma susceptibility. 18488026

2008
Entrez Id: 128869
Gene Symbol: PIGU
PIGU
CUI: C0025202
Disease: melanoma
melanoma 		0.110 GeneticVariation GWASDB Common sequence variants on 20q11.22 confer melanoma susceptibility. 18488026

2008
Entrez Id: 57644
Gene Symbol: MYH7B
MYH7B
CUI: C0025202
Disease: melanoma
melanoma 		0.110 GeneticVariation GWASDB Common sequence variants on 20q11.22 confer melanoma susceptibility. 18488026

2008
Entrez Id: 647979
Gene Symbol: NORAD
NORAD
CUI: C0025202
Disease: melanoma
melanoma 		0.110 GeneticVariation GWASDB Common sequence variants on 20q11.22 confer melanoma susceptibility. 18488026

2008
Entrez Id: 124045
Gene Symbol: SPATA33
SPATA33
CUI: C0025202
Disease: melanoma
melanoma 		0.100 GeneticVariation GWASDB A unique genome-wide association analysis in extended Utah high-risk pedigrees identifies a novel melanoma risk variant on chromosome arm 10q. 21706340

2012
Entrez Id: 172
Gene Symbol: AFG3L1P
AFG3L1P
CUI: C0025202
Disease: melanoma
melanoma 		0.100 GeneticVariation GWASDB Genome-wide association study identifies novel loci predisposing to cutaneous melanoma. 21926416

2011