rs4149601, NEDD4L

N. diseases: 8
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.
Cardiovascular Diseases
CUI: C0007222
Disease: Cardiovascular Diseases
711 0.882 0.160 18 58149559 splice region variant G/A snv 0.28 0.33 0.020 1.000 2 2011 2014
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
1085 0.882 0.160 18 58149559 splice region variant G/A snv 0.28 0.33 0.020 1.000 2 2008 2009
Attention deficit hyperactivity disorder
420 0.882 0.160 18 58149559 splice region variant G/A snv 0.28 0.33 0.010 1.000 1 2009 2009
Essential Hypertension
CUI: C0085580
Disease: Essential Hypertension
293 0.882 0.160 18 58149559 splice region variant G/A snv 0.28 0.33 0.010 1.000 1 2014 2014
Hypotension, Orthostatic
CUI: C0020651
Disease: Hypotension, Orthostatic
21 0.882 0.160 18 58149559 splice region variant G/A snv 0.28 0.33 0.010 1.000 1 2009 2009
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1641 0.882 0.160 18 58149559 splice region variant G/A snv 0.28 0.33 0.010 1.000 1 2014 2014
Obesity
CUI: C0028754
Disease: Obesity
1111 0.882 0.160 18 58149559 splice region variant G/A snv 0.28 0.33 0.010 1.000 1 2013 2013
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
1374 0.882 0.160 18 58149559 splice region variant G/A snv 0.28 0.33 0.010 1.000 1 2014 2014