rs744166, STAT3

N. diseases: 22
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.
Crohn Disease
CUI: C0010346
Disease: Crohn Disease
1147 0.689 0.560 17 42362183 intron variant A/G snv 0.48 0.870 1.000 8 2008 2016
Multiple Sclerosis
CUI: C0026769
Disease: Multiple Sclerosis
1022 0.689 0.560 17 42362183 intron variant A/G snv 0.48 0.820 1.000 2 2010 2012
Asthma
CUI: C0004096
Disease: Asthma
1536 0.689 0.560 17 42362183 intron variant A/G snv 0.48 0.700 1.000 1 2011 2011
Inflammatory Bowel Diseases
CUI: C0021390
Disease: Inflammatory Bowel Diseases
605 0.689 0.560 17 42362183 intron variant A/G snv 0.48 0.700 1.000 1 2015 2015
Ulcerative Colitis
CUI: C0009324
Disease: Ulcerative Colitis
827 0.689 0.560 17 42362183 intron variant A/G snv 0.48 0.030 1.000 3 2012 2014
Hashimoto Disease
CUI: C0677607
Disease: Hashimoto Disease
131 0.689 0.560 17 42362183 intron variant A/G snv 0.48 0.020 1.000 2 2014 2015
Malignant neoplasm of stomach
CUI: C0024623
Disease: Malignant neoplasm of stomach
615 0.689 0.560 17 42362183 intron variant A/G snv 0.48 0.020 1.000 2 2014 2015
Neoplasms
CUI: C0027651
Disease: Neoplasms
1644 0.689 0.560 17 42362183 intron variant A/G snv 0.48 0.020 1.000 2 2014 2016
Stomach Carcinoma
CUI: C0699791
Disease: Stomach Carcinoma
652 0.689 0.560 17 42362183 intron variant A/G snv 0.48 0.020 1.000 2 2014 2015
Aplastic Anemia
CUI: C0002874
Disease: Aplastic Anemia
30 0.689 0.560 17 42362183 intron variant A/G snv 0.48 0.010 1.000 1 2018 2018
Arthritis, Psoriatic
CUI: C0003872
Disease: Arthritis, Psoriatic
89 0.689 0.560 17 42362183 intron variant A/G snv 0.48 0.010 1.000 1 2013 2013
Behcet Syndrome
CUI: C0004943
Disease: Behcet Syndrome
243 0.689 0.560 17 42362183 intron variant A/G snv 0.48 0.010 1.000 1 2013 2013
Colon Carcinoma
CUI: C0699790
Disease: Colon Carcinoma
275 0.689 0.560 17 42362183 intron variant A/G snv 0.48 0.010 1.000 1 2014 2014
Gastritis
CUI: C0017152
Disease: Gastritis
21 0.689 0.560 17 42362183 intron variant A/G snv 0.48 0.010 1.000 1 2015 2015
Graves Disease
CUI: C0018213
Disease: Graves Disease
352 0.689 0.560 17 42362183 intron variant A/G snv 0.48 0.010 1.000 1 2015 2015
Laryngeal Squamous Cell Carcinoma
CUI: C0280324
Disease: Laryngeal Squamous Cell Carcinoma
30 0.689 0.560 17 42362183 intron variant A/G snv 0.48 0.010 1.000 1 2019 2019
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1641 0.689 0.560 17 42362183 intron variant A/G snv 0.48 0.010 1.000 1 2015 2015
Malignant tumor of colon
CUI: C0007102
Disease: Malignant tumor of colon
688 0.689 0.560 17 42362183 intron variant A/G snv 0.48 0.010 1.000 1 2014 2014
Non-Small Cell Lung Carcinoma
CUI: C0007131
Disease: Non-Small Cell Lung Carcinoma
712 0.689 0.560 17 42362183 intron variant A/G snv 0.48 0.010 1.000 1 2011 2011
Pituitary Adenoma
CUI: C0032000
Disease: Pituitary Adenoma
11 0.689 0.560 17 42362183 intron variant A/G snv 0.48 0.010 1.000 1 2017 2017
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
1374 0.689 0.560 17 42362183 intron variant A/G snv 0.48 0.010 1.000 1 2015 2015
Stomatitis
CUI: C0038362
Disease: Stomatitis
22 0.689 0.560 17 42362183 intron variant A/G snv 0.48 0.010 1.000 1 2017 2017