rs121909293, CTRC

N. diseases: 5
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Hereditary pancreatitis
CUI: C0238339
Disease: Hereditary pancreatitis
108 0.851 0.080 1 15445717 missense variant C/T snv 4.4E-03 3.8E-03 0.800 1.000 7 2008 2015
PANCREATITIS, CHRONIC, SUSCEPTIBILITY TO
3 0.851 0.080 1 15445717 missense variant C/T snv 4.4E-03 3.8E-03 0.700 0
Pancreatitis, Chronic
CUI: C0149521
Disease: Pancreatitis, Chronic
56 0.851 0.080 1 15445717 missense variant C/T snv 4.4E-03 3.8E-03 0.020 1.000 2 2010 2017
Hyperparathyroidism, Primary
CUI: C0221002
Disease: Hyperparathyroidism, Primary
39 0.851 0.080 1 15445717 missense variant C/T snv 4.4E-03 3.8E-03 0.010 1.000 1 2011 2011
Pancreatitis
CUI: C0030305
Disease: Pancreatitis
80 0.851 0.080 1 15445717 missense variant C/T snv 4.4E-03 3.8E-03 0.010 1.000 1 2011 2011