Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs139834892
rs139834892
0.882 0.040 19 43553481 missense variant C/T snv 6.4E-05 1.1E-04
Myelofibrosis due to another disorder
0.010 1.000 1 2018 2018
dbSNP: rs1799782
rs1799782
0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02
Myelofibrosis due to another disorder
0.010 1.000 1 2018 2018