rs1451011538, CRISPLD2

N. diseases: 2
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.
Hyperparathyroidism, Primary
CUI: C0221002
Disease: Hyperparathyroidism, Primary
39 0.925 0.080 16 84838647 missense variant T/A snv 4.0E-06 0.010 1.000 1 2008 2008
Pancreatitis
CUI: C0030305
Disease: Pancreatitis
80 0.925 0.080 16 84838647 missense variant T/A snv 4.0E-06 0.010 1.000 1 2008 2008