rs486907, RNASEL

N. diseases: 32
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Hereditary pancreatitis
CUI: C0238339
Disease: Hereditary pancreatitis
0.020 GeneticVariation BEFREE Cosegregation between the truncating mutation E265X and disease in a hereditary prostate cancer (HPC) family and association between prostate cancer risk and the common missense variant R462Q has been reported. 15534086 2004
Hereditary pancreatitis
CUI: C0238339
Disease: Hereditary pancreatitis
0.020 GeneticVariation BEFREE In addition, of the four missense variants found, R462Q showed an association with HPC (OR=1.96; P=.07). 11941539 2002