rs10974944, JAK2;INSL6

N. diseases: 4
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.
Myeloproliferative disease
CUI: C0027022
Disease: Myeloproliferative disease
43 0.882 0.160 9 5070831 intron variant C/G snv 0.25 0.810 1.000 2 2009 2010
Chronic myeloproliferative disorder
CUI: C1292778
Disease: Chronic myeloproliferative disorder
47 0.882 0.160 9 5070831 intron variant C/G snv 0.25 0.040 1.000 4 2009 2014
Primary Myelofibrosis
CUI: C0001815
Disease: Primary Myelofibrosis
29 0.882 0.160 9 5070831 intron variant C/G snv 0.25 0.010 1.000 1 2010 2010
Supraventricular tachycardia
CUI: C0039240
Disease: Supraventricular tachycardia
7 0.882 0.160 9 5070831 intron variant C/G snv 0.25 0.010 1.000 1 2014 2014