rs3184504, SH2B3;ATXN2

N. diseases: 29
Source: BEFREE ×
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.
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
547 0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 0.010 1.000 1 2018 2018
Primary malignant neoplasm of lung
CUI: C1306460
Disease: Primary malignant neoplasm of lung
981 0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 0.010 1.000 1 2015 2015
Primary Myelofibrosis
CUI: C0001815
Disease: Primary Myelofibrosis
25 0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 0.010 1.000 1 2016 2016
Thrombocythemia, Essential
CUI: C0040028
Disease: Thrombocythemia, Essential
32 0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 0.010 1.000 1 2016 2016