rs777418530, CRISPLD2

N. diseases: 10
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.
Pancreatitis
CUI: C0030305
Disease: Pancreatitis
80 0.763 0.120 16 84845883 missense variant A/G snv 4.0E-06 7.0E-06 0.040 1.000 4 2002 2020
Acute pancreatitis
CUI: C0001339
Disease: Acute pancreatitis
51 0.763 0.120 16 84845883 missense variant A/G snv 4.0E-06 7.0E-06 0.020 1.000 2 2005 2008
Diabetes
CUI: C0011847
Disease: Diabetes
710 0.763 0.120 16 84845883 missense variant A/G snv 4.0E-06 7.0E-06 0.020 1.000 2 2002 2002
Diabetes Mellitus
CUI: C0011849
Disease: Diabetes Mellitus
824 0.763 0.120 16 84845883 missense variant A/G snv 4.0E-06 7.0E-06 0.020 1.000 2 2002 2002
Pancreatitis, Chronic
CUI: C0149521
Disease: Pancreatitis, Chronic
56 0.763 0.120 16 84845883 missense variant A/G snv 4.0E-06 7.0E-06 0.020 1.000 2 2002 2010
TROPICAL CALCIFIC PANCREATITIS
CUI: C1842402
Disease: TROPICAL CALCIFIC PANCREATITIS
13 0.763 0.120 16 84845883 missense variant A/G snv 4.0E-06 7.0E-06 0.020 1.000 2 2002 2009
Diabetes Mellitus, Non-Insulin-Dependent
2672 0.763 0.120 16 84845883 missense variant A/G snv 4.0E-06 7.0E-06 0.010 1.000 1 2002 2002
Fibrocalculous pancreatic diabetes
CUI: C0271642
Disease: Fibrocalculous pancreatic diabetes
3 0.763 0.120 16 84845883 missense variant A/G snv 4.0E-06 7.0E-06 0.010 1.000 1 2002 2002
Hereditary pancreatitis
CUI: C0238339
Disease: Hereditary pancreatitis
108 0.763 0.120 16 84845883 missense variant A/G snv 4.0E-06 7.0E-06 0.010 1.000 1 2001 2001
Hyperparathyroidism, Primary
CUI: C0221002
Disease: Hyperparathyroidism, Primary
39 0.763 0.120 16 84845883 missense variant A/G snv 4.0E-06 7.0E-06 0.010 1.000 1 2008 2008