rs4364254, HPSE

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.
Acute GVH disease
CUI: C0856825
Disease: Acute GVH disease
49 0.882 0.080 4 83302560 intron variant C/T snv 0.63 0.010 1.000 1 2010 2010
Leukemia, Myelocytic, Acute
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
6892 0.882 0.080 4 83302560 intron variant C/T snv 0.63 0.010 1.000 1 2007 2007
Spondylo-ocular syndrome
CUI: C4225412
Disease: Spondylo-ocular syndrome
5 0.882 0.080 4 83302560 intron variant C/T snv 0.63 0.010 1.000 1 2015 2015