rs867770797, EDNRA

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.
Migraine Disorders
CUI: C0149931
Disease: Migraine Disorders
264 0.851 0.200 4 147519875 missense variant G/A snv 0.030 1.000 3 2001 2011
Cardiomyopathy, Dilated
CUI: C0007193
Disease: Cardiomyopathy, Dilated
509 0.851 0.200 4 147519875 missense variant G/A snv 0.010 1.000 1 2007 2007
Cardiomyopathy, Familial Idiopathic
CUI: C1449563
Disease: Cardiomyopathy, Familial Idiopathic
243 0.851 0.200 4 147519875 missense variant G/A snv 0.010 1.000 1 2007 2007
Disorder of eye
CUI: C0015397
Disease: Disorder of eye
14 0.851 0.200 4 147519875 missense variant G/A snv 0.010 1 2014 2014
Graves Disease
CUI: C0018213
Disease: Graves Disease
352 0.851 0.200 4 147519875 missense variant G/A snv 0.010 1 2014 2014
Hashimoto Disease
CUI: C0677607
Disease: Hashimoto Disease
131 0.851 0.200 4 147519875 missense variant G/A snv 0.010 1.000 1 2014 2014
Headache
CUI: C0018681
Disease: Headache
75 0.851 0.200 4 147519875 missense variant G/A snv 0.010 1.000 1 2006 2006
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
680 0.851 0.200 4 147519875 missense variant G/A snv 0.010 1.000 1 2009 2009