rs501192, CASP1

N. diseases: 3
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.
Acute Chest Syndrome
CUI: C0742343
Disease: Acute Chest Syndrome
135 0.925 0.200 11 105029658 splice region variant C/T snv 0.17 0.15 0.010 1.000 1 2017 2017
Cardiomyopathies
CUI: C0878544
Disease: Cardiomyopathies
294 0.925 0.200 11 105029658 splice region variant C/T snv 0.17 0.15 0.010 1.000 1 2017 2017
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
680 0.925 0.200 11 105029658 splice region variant C/T snv 0.17 0.15 0.010 1.000 1 2010 2010