Source: GWASDB

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs7023329
rs7023329
MTAP
CUI: C0025202
Disease: melanoma
melanoma 		0.810 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
dbSNP: rs17119461
rs17119461
LINC02627
CUI: C0025202
Disease: melanoma
melanoma 		0.810 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
dbSNP: rs258322
rs258322
CDK10
CUI: C0025202
Disease: melanoma
melanoma 		0.800 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
dbSNP: rs1393350
rs1393350
TYR ; LOC107984363
CUI: C0025202
Disease: melanoma
melanoma 		0.800 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
dbSNP: rs1335510
rs1335510
LOC107987026
CUI: C0025202
Disease: melanoma
melanoma 		0.710 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
dbSNP: rs132985
rs132985
PLA2G6
CUI: C0025202
Disease: melanoma
melanoma 		0.710 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
dbSNP: rs10757257
rs10757257
MTAP
CUI: C0025202
Disease: melanoma
melanoma 		0.710 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
dbSNP: rs8059973
rs8059973
DBNDD1
CUI: C0025202
Disease: melanoma
melanoma 		0.700 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
dbSNP: rs738322
rs738322
PLA2G6
CUI: C0025202
Disease: melanoma
melanoma 		0.700 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
dbSNP: rs7188458
rs7188458
SPATA33
CUI: C0025202
Disease: melanoma
melanoma 		0.700 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
dbSNP: rs4636294
rs4636294
LOC107987026
CUI: C0025202
Disease: melanoma
melanoma 		0.700 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
dbSNP: rs4238833
rs4238833
AFG3L1P
CUI: C0025202
Disease: melanoma
melanoma 		0.700 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
dbSNP: rs2353033
rs2353033
ANKRD11 ; LOC100287036
CUI: C0025202
Disease: melanoma
melanoma 		0.700 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
dbSNP: rs2218220
rs2218220
LOC107987026
CUI: C0025202
Disease: melanoma
melanoma 		0.700 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
dbSNP: rs1341866
rs1341866
CUI: C0025202
Disease: melanoma
melanoma 		0.700 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
dbSNP: rs16953002
rs16953002
FTO
CUI: C0025202
Disease: melanoma
melanoma 		A 0.800 GeneticVariation GWASDB A variant in FTO shows association with melanoma risk not due to BMI. 23455637

2013
dbSNP: rs4911442
rs4911442
NCOA6
CUI: C0025202
Disease: melanoma
melanoma 		0.720 GeneticVariation GWASDB Common sequence variants on 20q11.22 confer melanoma susceptibility. 18488026

2008
dbSNP: rs7271289
rs7271289
NCOA6
CUI: C0025202
Disease: melanoma
melanoma 		0.700 GeneticVariation GWASDB Common sequence variants on 20q11.22 confer melanoma susceptibility. 18488026

2008
dbSNP: rs721970
rs721970
CUI: C0025202
Disease: melanoma
melanoma 		0.700 GeneticVariation GWASDB Common sequence variants on 20q11.22 confer melanoma susceptibility. 18488026

2008
dbSNP: rs6058339
rs6058339
PHF20
CUI: C0025202
Disease: melanoma
melanoma 		0.700 GeneticVariation GWASDB Common sequence variants on 20q11.22 confer melanoma susceptibility. 18488026

2008
dbSNP: rs291671
rs291671
CDK5RAP1
CUI: C0025202
Disease: melanoma
melanoma 		0.700 GeneticVariation GWASDB Common sequence variants on 20q11.22 confer melanoma susceptibility. 18488026

2008
dbSNP: rs17305657
rs17305657
BPIFA3
CUI: C0025202
Disease: melanoma
melanoma 		0.700 GeneticVariation GWASDB Common sequence variants on 20q11.22 confer melanoma susceptibility. 18488026

2008
dbSNP: rs1204552
rs1204552
NORAD
CUI: C0025202
Disease: melanoma
melanoma 		0.700 GeneticVariation GWASDB Common sequence variants on 20q11.22 confer melanoma susceptibility. 18488026

2008
dbSNP: rs7412746
rs7412746
CTXND2
CUI: C0025202
Disease: melanoma
melanoma 		T 0.800 GeneticVariation GWASDB Genome-wide association study identifies a new melanoma susceptibility locus at 1q21.3. 21983785

2011
dbSNP: rs258322
rs258322
CDK10
CUI: C0025202
Disease: melanoma
melanoma 		0.800 GeneticVariation GWASDB Genome-wide association study identifies novel loci predisposing to cutaneous melanoma. 21926416

2011