rs10974947, INSL6;JAK2

N. diseases: 3
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.
Primary Myelofibrosis
CUI: C0001815
Disease: Primary Myelofibrosis
29 0.882 0.080 9 5072846 intron variant G/A snv 0.23 0.010 1.000 1 2008 2008
Thrombocythemia, Essential
CUI: C0040028
Disease: Thrombocythemia, Essential
37 0.882 0.080 9 5072846 intron variant G/A snv 0.23 0.010 1.000 1 2008 2008
Polycythemia Vera
CUI: C0032463
Disease: Polycythemia Vera
38 0.882 0.080 9 5072846 intron variant G/A snv 0.23 0.010 1.000 1 2008 2008