rs4917014, None

N. diseases: 8
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.
Lupus Erythematosus, Systemic
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
1172 0.807 0.360 7 50266267 upstream gene variant T/G snv 0.26 0.830 1.000 6 2009 2017
High density lipoprotein measurement
CUI: C0392885
Disease: High density lipoprotein measurement
1440 0.807 0.360 7 50266267 upstream gene variant T/G snv 0.26 0.800 1.000 3 2013 2018
Serum HDL cholesterol measurement
CUI: C0428472
Disease: Serum HDL cholesterol measurement
679 0.807 0.360 7 50266267 upstream gene variant T/G snv 0.26 0.700 1.000 1 2013 2013
Stevens-Johnson Syndrome
CUI: C0038325
Disease: Stevens-Johnson Syndrome
16 0.807 0.360 7 50266267 upstream gene variant T/G snv 0.26 0.700 1.000 1 2015 2015
Toxic Epidermal Necrolysis
CUI: C0014518
Disease: Toxic Epidermal Necrolysis
29 0.807 0.360 7 50266267 upstream gene variant T/G snv 0.26 0.700 1.000 1 2015 2015
Nephritis
CUI: C0027697
Disease: Nephritis
40 0.807 0.360 7 50266267 upstream gene variant T/G snv 0.26 0.010 1.000 1 2010 2010
Primary Sjögren's syndrome
CUI: C0151449
Disease: Primary Sjögren's syndrome
42 0.807 0.360 7 50266267 upstream gene variant T/G snv 0.26 0.010 1.000 1 2017 2017
Vasculitis
CUI: C0042384
Disease: Vasculitis
24 0.807 0.360 7 50266267 upstream gene variant T/G snv 0.26 0.010 1.000 1 2010 2010