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.
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
Human papilloma virus infection
CUI: C0343641
Disease: Human papilloma virus infection
42 0.620 0.680 X 49261784 intron variant G/A;T snv 0.010 1.000 1 2019 2019
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
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
Malignant neoplasm of endometrium
CUI: C0007103
Disease: Malignant neoplasm of endometrium
197 0.620 0.680 X 49261784 intron variant G/A;T snv 0.010 1.000 1 2018 2018
Malignant neoplasm of prostate
CUI: C0376358
Disease: Malignant neoplasm of prostate
1082 0.620 0.680 X 49261784 intron variant G/A;T snv 0.010 1.000 1 2019 2019
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
Osteoarthritis, Knee
CUI: C0409959
Disease: Osteoarthritis, Knee
150 0.620 0.680 X 49261784 intron variant G/A;T snv 0.010 1.000 1 2018 2018
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
Peptic Ulcer
CUI: C0030920
Disease: Peptic Ulcer
25 0.620 0.680 X 49261784 intron variant G/A;T snv 0.010 1.000 1 2018 2018
Prostate carcinoma
CUI: C0600139
Disease: Prostate carcinoma
1168 0.620 0.680 X 49261784 intron variant G/A;T snv 0.010 1.000 1 2019 2019
Psoriasis
CUI: C0033860
Disease: Psoriasis
705 0.620 0.680 X 49261784 intron variant G/A;T snv 0.010 1 2017 2017
Squamous intraepithelial lesion
CUI: C0333873
Disease: Squamous intraepithelial lesion
8 0.620 0.680 X 49261784 intron variant G/A;T snv 0.010 1.000 1 2019 2019
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
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
Tumor Cell Invasion
CUI: C1269955
Disease: Tumor Cell Invasion
169 0.620 0.680 X 49261784 intron variant G/A;T snv 0.010 1.000 1 2018 2018