rs1044498, ENPP1

N. diseases: 15
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.
Diabetes Mellitus, Non-Insulin-Dependent
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
2672 0.752 0.360 6 131851228 missense variant A/C;G snv 0.19 0.100 0.800 10 2009 2019
Obesity
CUI: C0028754
Disease: Obesity
1111 0.752 0.360 6 131851228 missense variant A/C;G snv 0.19 0.040 1.000 4 2008 2019
Diabetic Nephropathy
CUI: C0011881
Disease: Diabetic Nephropathy
238 0.752 0.360 6 131851228 missense variant A/C;G snv 0.19 0.020 1.000 2 2011 2015
Bone Diseases
CUI: C0005940
Disease: Bone Diseases
10 0.752 0.360 6 131851228 missense variant A/C;G snv 0.19 0.010 1.000 1 2017 2017
Cardiovascular Diseases
CUI: C0007222
Disease: Cardiovascular Diseases
711 0.752 0.360 6 131851228 missense variant A/C;G snv 0.19 0.010 1.000 1 2011 2011
Cerebrovascular accident
CUI: C0038454
Disease: Cerebrovascular accident
591 0.752 0.360 6 131851228 missense variant A/C;G snv 0.19 0.010 1.000 1 2013 2013
Chronic kidney disease stage 5
CUI: C2316810
Disease: Chronic kidney disease stage 5
194 0.752 0.360 6 131851228 missense variant A/C;G snv 0.19 0.010 1 2008 2008
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
1962 0.752 0.360 6 131851228 missense variant A/C;G snv 0.19 0.010 1.000 1 2012 2012
Diabetes
CUI: C0011847
Disease: Diabetes
710 0.752 0.360 6 131851228 missense variant A/C;G snv 0.19 0.010 1.000 1 2011 2011
Diabetes Mellitus
CUI: C0011849
Disease: Diabetes Mellitus
824 0.752 0.360 6 131851228 missense variant A/C;G snv 0.19 0.010 1.000 1 2011 2011
Kidney Diseases
CUI: C0022658
Disease: Kidney Diseases
140 0.752 0.360 6 131851228 missense variant A/C;G snv 0.19 0.010 1.000 1 2011 2011
Kidney Failure
CUI: C0035078
Disease: Kidney Failure
36 0.752 0.360 6 131851228 missense variant A/C;G snv 0.19 0.010 1 2008 2008
Kidney Failure, Chronic
CUI: C0022661
Disease: Kidney Failure, Chronic
425 0.752 0.360 6 131851228 missense variant A/C;G snv 0.19 0.010 1 2008 2008
Non-alcoholic Fatty Liver Disease
CUI: C0400966
Disease: Non-alcoholic Fatty Liver Disease
222 0.752 0.360 6 131851228 missense variant A/C;G snv 0.19 0.010 1.000 1 2019 2019
Pachyonychia Congenita, Jadassohn Lewandowsky Type
CUI: C1706595
Disease: Pachyonychia Congenita, Jadassohn Lewandowsky Type
19 0.752 0.360 6 131851228 missense variant A/C;G snv 0.19 0.010 1.000 1 2008 2008