rs2282015, LINC02641

N. diseases: 2
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.
Leukemia, Myelocytic, Acute
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
6892 1.000 0.040 10 123462521 intron variant T/G snv 0.39 0.700 1.000 1 2017 2017
Venous Thromboembolism
CUI: C1861172
Disease: Venous Thromboembolism
408 1.000 0.040 10 123462521 intron variant T/G snv 0.39 0.700 1.000 1 2013 2013