rs3761548, FOXP3

N. diseases: 42
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.
Breast Carcinoma
CUI: C0678222
Disease: Breast Carcinoma
2793 0.620 0.680 X 49261784 intron variant G/A;T snv 0.040 1.000 4 2014 2019
Malignant neoplasm of breast
CUI: C0006142
Disease: Malignant neoplasm of breast
3417 0.620 0.680 X 49261784 intron variant G/A;T snv 0.040 1.000 4 2014 2019
Multiple Sclerosis
CUI: C0026769
Disease: Multiple Sclerosis
1022 0.620 0.680 X 49261784 intron variant G/A;T snv 0.040 1.000 4 2015 2019
Allergic rhinitis (disorder)
CUI: C2607914
Disease: Allergic rhinitis (disorder)
176 0.620 0.680 X 49261784 intron variant G/A;T snv 0.030 0.667 3 2011 2017
Acute Chest Syndrome
CUI: C0742343
Disease: Acute Chest Syndrome
135 0.620 0.680 X 49261784 intron variant G/A;T snv 0.020 1.000 2 2013 2016
Autoimmune Diseases
CUI: C0004364
Disease: Autoimmune Diseases
428 0.620 0.680 X 49261784 intron variant G/A;T snv 0.020 1.000 2 2013 2013
Graves Disease
CUI: C0018213
Disease: Graves Disease
352 0.620 0.680 X 49261784 intron variant G/A;T snv 0.020 1.000 2 2013 2019
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1641 0.620 0.680 X 49261784 intron variant G/A;T snv 0.020 1.000 2 2018 2019
Neoplasms
CUI: C0027651
Disease: Neoplasms
1644 0.620 0.680 X 49261784 intron variant G/A;T snv 0.020 1.000 2 2014 2018
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
1374 0.620 0.680 X 49261784 intron variant G/A;T snv 0.020 1.000 2 2018 2019
Tumor Progression
CUI: C0178874
Disease: Tumor Progression
72 0.620 0.680 X 49261784 intron variant G/A;T snv 0.020 1.000 2 2014 2018
Vitiligo
CUI: C0042900
Disease: Vitiligo
249 0.620 0.680 X 49261784 intron variant G/A;T snv 0.020 1.000 2 2013 2013
VITILIGO-ASSOCIATED MULTIPLE AUTOIMMUNE DISEASE SUSCEPTIBILITY 1 (finding)
92 0.620 0.680 X 49261784 intron variant G/A;T snv 0.020 1.000 2 2013 2013
Autism Spectrum Disorders
CUI: C1510586
Disease: Autism Spectrum Disorders
331 0.620 0.680 X 49261784 intron variant G/A;T snv 0.010 1 2017 2017
Autoimmune thyroid disease (AITD)
CUI: C3840565
Disease: Autoimmune thyroid disease (AITD)
54 0.620 0.680 X 49261784 intron variant G/A;T snv 0.010 1 2019 2019
Chronic kidney disease stage 5
CUI: C2316810
Disease: Chronic kidney disease stage 5
194 0.620 0.680 X 49261784 intron variant G/A;T snv 0.010 1.000 1 2016 2016
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
1962 0.620 0.680 X 49261784 intron variant G/A;T snv 0.010 1.000 1 2014 2014
Crohn Disease
CUI: C0010346
Disease: Crohn Disease
1147 0.620 0.680 X 49261784 intron variant G/A;T snv 0.010 1.000 1 2019 2019
Cytomegalovirus Infections
CUI: C0010823
Disease: Cytomegalovirus Infections
26 0.620 0.680 X 49261784 intron variant G/A;T snv 0.010 1.000 1 2016 2016
Degenerative polyarthritis
CUI: C0029408
Disease: Degenerative polyarthritis
247 0.620 0.680 X 49261784 intron variant G/A;T snv 0.010 1.000 1 2018 2018
Endometrial Carcinoma
CUI: C0476089
Disease: Endometrial Carcinoma
326 0.620 0.680 X 49261784 intron variant G/A;T snv 0.010 1.000 1 2018 2018
Endometriosis
CUI: C0014175
Disease: Endometriosis
274 0.620 0.680 X 49261784 intron variant G/A;T snv 0.010 1.000 1 2011 2011
Graft-vs-Host Disease
CUI: C0018133
Disease: Graft-vs-Host Disease
25 0.620 0.680 X 49261784 intron variant G/A;T snv 0.010 1 2016 2016
Hashimoto Disease
CUI: C0677607
Disease: Hashimoto Disease
131 0.620 0.680 X 49261784 intron variant G/A;T snv 0.010 1.000 1 2019 2019
Helicobacter pylori (H. pylori) infection in conditions classified elsewhere and of unspecified site
24 0.620 0.680 X 49261784 intron variant G/A;T snv 0.010 1.000 1 2018 2018