rs1070073, STAB2

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.
Factor VIII measurement
CUI: C2825857
Disease: Factor VIII measurement
42 12 103606541 intron variant T/G snv 0.71 0.700 1.000 1 2019 2019
von Willebrand's factor (lab test)
CUI: C2239219
Disease: von Willebrand's factor (lab test)
427 12 103606541 intron variant T/G snv 0.71 0.700 1.000 1 2019 2019