rs10050860, ERAP1

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.
Ankylosing spondylitis
CUI: C0038013
Disease: Ankylosing spondylitis
609 0.882 0.240 5 96786506 missense variant C/T snv 0.15 0.16 0.790 0.900 10 2010 2019
Behcet Syndrome
CUI: C0004943
Disease: Behcet Syndrome
243 0.882 0.240 5 96786506 missense variant C/T snv 0.15 0.16 0.020 1.000 2 2015 2015
Spondylarthritis
CUI: C0949690
Disease: Spondylarthritis
23 0.882 0.240 5 96786506 missense variant C/T snv 0.15 0.16 0.020 1.000 2 2013 2015
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
1085 0.882 0.240 5 96786506 missense variant C/T snv 0.15 0.16 0.010 1.000 1 2018 2018