rs3783613, VCAM1

N. diseases: 6
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.
Cerebrovascular accident
CUI: C0038454
Disease: Cerebrovascular accident
591 0.851 0.200 1 100731231 missense variant G/A;C snv 4.0E-06; 9.9E-03 0.020 0.500 2 2002 2015
alpha-Thalassemia
CUI: C0002312
Disease: alpha-Thalassemia
37 0.851 0.200 1 100731231 missense variant G/A;C snv 4.0E-06; 9.9E-03 0.010 1.000 1 2015 2015
alpha^+^ Thalassemia
CUI: C1456873
Disease: alpha^+^ Thalassemia
16 0.851 0.200 1 100731231 missense variant G/A;C snv 4.0E-06; 9.9E-03 0.010 1.000 1 2015 2015
Anemia, Sickle Cell
CUI: C0002895
Disease: Anemia, Sickle Cell
138 0.851 0.200 1 100731231 missense variant G/A;C snv 4.0E-06; 9.9E-03 0.010 1.000 1 2015 2015
Cerebrovascular Disorders
CUI: C0007820
Disease: Cerebrovascular Disorders
56 0.851 0.200 1 100731231 missense variant G/A;C snv 4.0E-06; 9.9E-03 0.010 1.000 1 2015 2015
Rheumatoid Arthritis
CUI: C0003873
Disease: Rheumatoid Arthritis
2387 0.851 0.200 1 100731231 missense variant G/A;C snv 4.0E-06; 9.9E-03 0.010 1.000 1 2009 2009