Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs198977
rs198977
0.040 GeneticVariation BEFREE The T allele of rs198977, a single nucleotide polymorphism in exon 5 of KLK2, codes for W-hK2 and is associated with lower serum hK2 levels and higher risk of prostate cancer than the C allele encoding R-hK2. 25847286

2015

dbSNP: rs198977
rs198977
0.040 GeneticVariation BEFREE This exploratory analysis in prostate cancer patients revealed the W allele of the KLK2 R250W SNP to be less likely associated with low GS morphology. 21178268

2010

dbSNP: rs198977
rs198977
0.040 GeneticVariation BEFREE Among the SNPs studied, the A allele of the KLK2-SNP1 (G>A, rs2664155) and the T allele of the KLK2-SNP5 (C>T, rs198977) polymorphisms showed positive associations with prostate cancer, adjusted ORs for KLK2-SNP1 AG and AA genotypes being 1.4 [95% confidence interval (95% CI), 1.2-1.8; P=0.002] and for KLK2-SNP5 TT or CT genotypes being 1.3 (95% CI, 1.1-1.6; P=0.05). 17085659

2006

dbSNP: rs198977
rs198977
0.040 GeneticVariation BEFREE Our results suggest that the C allele of the functional C748T polymorphism of KLK2 may increase the risk of PCa. 15643194

2005