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: rs121913615
rs121913615
0.683 0.240 1 43349338 missense variant G/C;T snv 8.0E-06
CUI: C0027022
Disease: Myeloproliferative disease
Myeloproliferative disease
Hemic and Lymphatic Diseases 0.070 1.000 7 2008 2019
dbSNP: rs121913616
rs121913616
0.790 0.120 1 43349337 missense variant TG/AA mnv
CUI: C0027022
Disease: Myeloproliferative disease
Myeloproliferative disease
Hemic and Lymphatic Diseases 0.020 1.000 2 2009 2017
dbSNP: rs1476891431
rs1476891431
1 43337895 missense variant C/T snv
CUI: C0027022
Disease: Myeloproliferative disease
Myeloproliferative disease
Hemic and Lymphatic Diseases 0.010 1.000 1 2016 2016