rs7582694, STAT4

N. diseases: 9
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 0.763 0.400 2 191105394 intron variant C/G snv 0.77 0.740 1.000 6 2008 2017
Primary Sjögren's syndrome
CUI: C0151449
Disease: Primary Sjögren's syndrome
42 0.763 0.400 2 191105394 intron variant C/G snv 0.77 0.010 1.000 1 2010 2010
Kidney Failure
CUI: C0035078
Disease: Kidney Failure
36 0.763 0.400 2 191105394 intron variant C/G snv 0.77 0.010 1.000 1 2013 2013
Renal Insufficiency
CUI: C1565489
Disease: Renal Insufficiency
42 0.763 0.400 2 191105394 intron variant C/G snv 0.77 0.010 1.000 1 2013 2013
Hepatitis B
CUI: C0019163
Disease: Hepatitis B
519 0.763 0.400 2 191105394 intron variant C/G snv 0.77 0.010 1.000 1 2015 2015
Endometriosis
CUI: C0014175
Disease: Endometriosis
274 0.763 0.400 2 191105394 intron variant C/G snv 0.77 0.020 1.000 2 2016 2019
Autoimmune Chronic Hepatitis
CUI: C0241910
Disease: Autoimmune Chronic Hepatitis
23 0.763 0.400 2 191105394 intron variant C/G snv 0.77 0.010 1.000 1 2017 2017
Autoimmune hepatitis
CUI: C4721555
Disease: Autoimmune hepatitis
22 0.763 0.400 2 191105394 intron variant C/G snv 0.77 0.010 1.000 1 2017 2017
Hypothyroidism
CUI: C0020676
Disease: Hypothyroidism
283 0.763 0.400 2 191105394 intron variant C/G snv 0.77 0.700 1.000 1 2019 2019