Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs187843643
rs187843643
Entrez Id: 102723526
Gene Symbol: LINC02218
LINC02218
CUI: C0025202
Disease:
melanoma
0.710 GeneticVariation BEFREE In addition, we uncover a novel polymorphism, rs187843643 (OR = 1.96; 95% CI = [1.54, 2.48]; P = 3.53 x 10-8), associated with melanoma. 28212542 2017
dbSNP: rs187843643
rs187843643
Entrez Id: 102723526
Gene Symbol: LINC02218
LINC02218
CUI: C0025202
Disease:
melanoma
T 0.710 GeneticVariation GWASCAT In addition, we uncover a novel polymorphism, rs187843643 (OR = 1.96; 95% CI = [1.54, 2.48]; P = 3.53 x 10-8), associated with melanoma. 28212542 2017