Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs748405415
rs748405415
Entrez Id: 5645
Gene Symbol: PRSS2
PRSS2
CUI: C0810032
Disease:
Pancreatic disorders (not diabetes)
0.010 GeneticVariation BEFREE A loss-of-function p.G191R variant in the anionic trypsinogen (PRSS2) gene in Japanese patients with pancreatic disorders. 19052022 2009