rs2284063, PLA2G6

N. diseases: 4
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
melanoma
CUI: C0025202
Disease: melanoma
0.800 GeneticVariation GWASCAT Two-stage genome-wide association study identifies a novel susceptibility locus associated with melanoma. 28212542 2017
melanoma
CUI: C0025202
Disease: melanoma
0.800 GeneticVariation GWASCAT Genome-wide association study identifies three loci associated with melanoma risk. 19578364 2009
Nevus
CUI: C0027960
Disease: Nevus
0.800 GeneticVariation GWASDB Genome-wide association study identifies variants at 9p21 and 22q13 associated with development of cutaneous nevi. 19578365 2009
melanoma
CUI: C0025202
Disease: melanoma
0.800 GeneticVariation GWASDB Genome-wide association study identifies three loci associated with melanoma risk. 19578364 2009
Nevus
CUI: C0027960
Disease: Nevus
0.800 GeneticVariation GWASCAT Genome-wide association study identifies variants at 9p21 and 22q13 associated with development of cutaneous nevi. 19578365 2009
Nasopharyngeal carcinoma
CUI: C2931822
Disease: Nasopharyngeal carcinoma
0.700 GeneticVariation GWASDB A genome-wide association study of nasopharyngeal carcinoma identifies three new susceptibility loci. 20512145 2010
Parkinson Disease
CUI: C0030567
Disease: Parkinson Disease
0.010 GeneticVariation BEFREE We found that the rs132985 A-rs2284063 C haplotype is marginally associated with increased risk of developing PD (P = 0.048) after 10,000 permutations. 22459563 2012