rs12342421, JAK2;INSL6

N. diseases: 5
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.
Chronic myeloproliferative disorder
CUI: C1292778
Disease: Chronic myeloproliferative disorder
47 0.851 0.080 9 5065750 intron variant G/C snv 0.23 0.020 1.000 2 2013 2014
Polycythemia Vera
CUI: C0032463
Disease: Polycythemia Vera
38 0.851 0.080 9 5065750 intron variant G/C snv 0.23 0.010 1.000 1 2008 2008
Primary Myelofibrosis
CUI: C0001815
Disease: Primary Myelofibrosis
29 0.851 0.080 9 5065750 intron variant G/C snv 0.23 0.010 1.000 1 2008 2008
Red Blood Cell Count measurement
CUI: C0014772
Disease: Red Blood Cell Count measurement
1599 0.851 0.080 9 5065750 intron variant G/C snv 0.23 0.700 1.000 1 2019 2019
Thrombocythemia, Essential
CUI: C0040028
Disease: Thrombocythemia, Essential
37 0.851 0.080 9 5065750 intron variant G/C snv 0.23 0.010 1.000 1 2008 2008