Source: BEFREE

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs3761548
rs3761548
FOXP3
0.620 0.680 X 49261784 intron variant G/A;T snv
CUI: C0374997
Disease: Helicobacter pylori (H. pylori) infection in conditions classified elsewhere and of unspecified site
Helicobacter pylori (H. pylori) infection in conditions classified elsewhere and of unspecified site 		0.010 1.000 1 2018 2018
dbSNP: rs3761548
rs3761548
FOXP3
0.620 0.680 X 49261784 intron variant G/A;T snv
CUI: C0022661
Disease: Kidney Failure, Chronic
Kidney Failure, Chronic 		0.010 1.000 1 2016 2016
dbSNP: rs3761548
rs3761548
FOXP3
0.620 0.680 X 49261784 intron variant G/A;T snv
CUI: C4722518
Disease: Triple-Negative Breast Carcinoma
Triple-Negative Breast Carcinoma 		0.010 1.000 1 2014 2014
dbSNP: rs3761548
rs3761548
FOXP3
0.620 0.680 X 49261784 intron variant G/A;T snv
CUI: C3539878
Disease: Triple Negative Breast Neoplasms
Triple Negative Breast Neoplasms 		0.010 1.000 1 2014 2014
dbSNP: rs3761548
rs3761548
FOXP3
0.620 0.680 X 49261784 intron variant G/A;T snv
CUI: C0007103
Disease: Malignant neoplasm of endometrium
Malignant neoplasm of endometrium 		0.010 1.000 1 2018 2018
dbSNP: rs3761548
rs3761548
FOXP3
0.620 0.680 X 49261784 intron variant G/A;T snv
CUI: C0263313
Disease: Pemphigus Foliaceus
Pemphigus Foliaceus 		0.010 1.000 1 2017 2017
dbSNP: rs3761548
rs3761548
FOXP3
0.620 0.680 X 49261784 intron variant G/A;T snv
CUI: C0030920
Disease: Peptic Ulcer
Peptic Ulcer 		0.010 1.000 1 2018 2018
dbSNP: rs3761548
rs3761548
FOXP3
0.620 0.680 X 49261784 intron variant G/A;T snv
CUI: C0409959
Disease: Osteoarthritis, Knee
Osteoarthritis, Knee 		0.010 1.000 1 2018 2018
dbSNP: rs3761548
rs3761548
FOXP3
0.620 0.680 X 49261784 intron variant G/A;T snv
CUI: C1269955
Disease: Tumor Cell Invasion
Tumor Cell Invasion 		0.010 1.000 1 2018 2018
dbSNP: rs3761548
rs3761548
FOXP3
0.620 0.680 X 49261784 intron variant G/A;T snv
CUI: C0343641
Disease: Human papilloma virus infection
Human papilloma virus infection 		0.010 1.000 1 2019 2019
dbSNP: rs3761548
rs3761548
FOXP3
0.620 0.680 X 49261784 intron variant G/A;T snv
CUI: C0019156
Disease: Hepatic Veno-Occlusive Disease
Hepatic Veno-Occlusive Disease 		0.010 1.000 1 2016 2016
dbSNP: rs3761548
rs3761548
FOXP3
0.620 0.680 X 49261784 intron variant G/A;T snv
CUI: C0333873
Disease: Squamous intraepithelial lesion
Squamous intraepithelial lesion 		0.010 1.000 1 2019 2019
dbSNP: rs3761548
rs3761548
FOXP3
0.620 0.680 X 49261784 intron variant G/A;T snv
CUI: C0010823
Disease: Cytomegalovirus Infections
Cytomegalovirus Infections 		0.010 1.000 1 2016 2016
dbSNP: rs3761548
rs3761548
FOXP3
0.620 0.680 X 49261784 intron variant G/A;T snv
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma 		0.010 1.000 1 2019 2019
dbSNP: rs3761548
rs3761548
FOXP3
0.620 0.680 X 49261784 intron variant G/A;T snv
CUI: C0677607
Disease: Hashimoto Disease
Hashimoto Disease 		0.010 1.000 1 2019 2019
dbSNP: rs3761548
rs3761548
FOXP3
0.620 0.680 X 49261784 intron variant G/A;T snv
CUI: C0014175
Disease: Endometriosis
Endometriosis 		0.010 1.000 1 2011 2011
dbSNP: rs3761548
rs3761548
FOXP3
0.620 0.680 X 49261784 intron variant G/A;T snv
CUI: C0476089
Disease: Endometrial Carcinoma
Endometrial Carcinoma 		0.010 1.000 1 2018 2018