rs4693608, HPSE

N. diseases: 6
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.
Acute GVH disease
CUI: C0856825
Disease: Acute GVH disease
49 0.827 0.200 4 83320204 intron variant G/A;C snv 0.020 1.000 2 2010 2014
Graft-vs-Host Disease
CUI: C0018133
Disease: Graft-vs-Host Disease
25 0.827 0.200 4 83320204 intron variant G/A;C snv 0.010 1.000 1 2018 2018
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1641 0.827 0.200 4 83320204 intron variant G/A;C snv 0.010 1.000 1 2018 2018
Multiple Myeloma
CUI: C0026764
Disease: Multiple Myeloma
865 0.827 0.200 4 83320204 intron variant G/A;C snv 0.010 1.000 1 2015 2015
Secondary malignant neoplasm of lymph node
CUI: C0686619
Disease: Secondary malignant neoplasm of lymph node
188 0.827 0.200 4 83320204 intron variant G/A;C snv 0.010 1.000 1 2012 2012
Spondylo-ocular syndrome
CUI: C4225412
Disease: Spondylo-ocular syndrome
5 0.827 0.200 4 83320204 intron variant G/A;C snv 0.010 1.000 1 2015 2015