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
0.801 0.107 1 43349308 missense variant G/A snp
CUI: C1292778
Disease: Chronic myeloproliferative disorder
Chronic myeloproliferative disorder
0.700 3 2008 2013
dbSNP: rs1057519752
rs1057519752
1.000 0.071 1 43349307 missense variant A/G,T snp
CUI: C1292778
Disease: Chronic myeloproliferative disorder
Chronic myeloproliferative disorder
0.700 1 2011 2011
dbSNP: rs121913615
rs121913615
0.734 0.179 1 43349338 missense variant G/C,T snp 8.0E-06
CUI: C1292778
Disease: Chronic myeloproliferative disorder
Chronic myeloproliferative disorder
0.060 1.000 6 2008 2014
dbSNP: rs121913616
rs121913616
0.821 0.107 1 43349337 missense variant TG/AA multinucleotide-polymorphism
CUI: C1292778
Disease: Chronic myeloproliferative disorder
Chronic myeloproliferative disorder
0.020 1.000 2 2008 2009
dbSNP: rs17292650
rs17292650
0.923 0.071 1 43338136 missense variant G/T snp 3.5E-03 1.3E-02
CUI: C1292778
Disease: Chronic myeloproliferative disorder
Chronic myeloproliferative disorder
0.010 1.000 1 2004 2004