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.
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
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
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
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)
CUI: C1847835
Disease: 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
Non-Small Cell Lung Carcinoma
CUI: C0007131
Disease: Non-Small Cell Lung Carcinoma
712 0.620 0.680 X 49261784 intron variant G/A;T snv 0.010 1.000 1 2013 2013
Systemic Scleroderma
CUI: C0036421
Disease: Systemic Scleroderma
287 0.620 0.680 X 49261784 intron variant G/A;T snv 0.010 1 2013 2013
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
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
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
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
Malignant neoplasm of colon and/or rectum
CUI: C4722085
Disease: Malignant neoplasm of colon and/or rectum
502 0.620 0.680 X 49261784 intron variant G/A;T snv 0.010 1.000 1 2014 2014
Triple Negative Breast Neoplasms
CUI: C3539878
Disease: Triple Negative Breast Neoplasms
99 0.620 0.680 X 49261784 intron variant G/A;T snv 0.010 1.000 1 2014 2014
Triple-Negative Breast Carcinoma
CUI: C4722518
Disease: Triple-Negative Breast Carcinoma
96 0.620 0.680 X 49261784 intron variant G/A;T snv 0.010 1.000 1 2014 2014
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
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
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
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
Hepatic Veno-Occlusive Disease
CUI: C0019156
Disease: Hepatic Veno-Occlusive Disease
2 0.620 0.680 X 49261784 intron variant G/A;T snv 0.010 1.000 1 2016 2016
Kidney Failure, Chronic
CUI: C0022661
Disease: Kidney Failure, Chronic
425 0.620 0.680 X 49261784 intron variant G/A;T snv 0.010 1.000 1 2016 2016
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
Pemphigus Foliaceus
CUI: C0263313
Disease: Pemphigus Foliaceus
16 0.620 0.680 X 49261784 intron variant G/A;T snv 0.010 1.000 1 2017 2017