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: rs121913614
rs121913614
0.790 0.120 1 43349308 missense variant G/A snv
CUI: C1292778
Disease: Chronic myeloproliferative disorder
Chronic myeloproliferative disorder
Neoplasms; Hemic and Lymphatic Diseases 0.710 1.000 4 2008 2013
dbSNP: rs121913616
rs121913616
0.790 0.120 1 43349337 missense variant TG/AA mnv
CUI: C1292778
Disease: Chronic myeloproliferative disorder
Chronic myeloproliferative disorder
Neoplasms; Hemic and Lymphatic Diseases 0.020 1.000 2 2008 2009
dbSNP: rs1057519752
rs1057519752
1.000 0.080 1 43349307 missense variant A/C;G;T snv
CUI: C1292778
Disease: Chronic myeloproliferative disorder
Chronic myeloproliferative disorder
Neoplasms; Hemic and Lymphatic Diseases 0.700 1.000 1 2011 2011
dbSNP: rs17292650
rs17292650
0.882 0.120 1 43338136 missense variant G/T snv 3.5E-03 1.4E-02
CUI: C1292778
Disease: Chronic myeloproliferative disorder
Chronic myeloproliferative disorder
Neoplasms; Hemic and Lymphatic Diseases 0.010 1.000 1 2004 2004
dbSNP: rs121913615
rs121913615
0.683 0.240 1 43349338 missense variant G/C;T snv 8.0E-06
CUI: C1292778
Disease: Chronic myeloproliferative disorder
Chronic myeloproliferative disorder
Neoplasms; Hemic and Lymphatic Diseases 0.100 1.000 10 2008 2018