rs2232365, FOXP3

N. diseases: 16
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 0.716 0.480 X 49259429 intron variant T/C snv 0.010 1 2017 2017
Acute GVH disease
CUI: C0856825
Disease: Acute GVH disease
49 0.716 0.480 X 49259429 intron variant T/C snv 0.010 1.000 1 2018 2018
Autism Spectrum Disorders
CUI: C1510586
Disease: Autism Spectrum Disorders
331 0.716 0.480 X 49259429 intron variant T/C snv 0.010 1.000 1 2017 2017
Breast Carcinoma
CUI: C0678222
Disease: Breast Carcinoma
2793 0.716 0.480 X 49259429 intron variant T/C snv 0.010 1.000 1 2017 2017
Chronic kidney disease stage 5
CUI: C2316810
Disease: Chronic kidney disease stage 5
194 0.716 0.480 X 49259429 intron variant T/C snv 0.010 1.000 1 2016 2016
Congenital chromosomal disease
CUI: C0008626
Disease: Congenital chromosomal disease
47 0.716 0.480 X 49259429 intron variant T/C snv 0.010 1.000 1 2018 2018
Degenerative polyarthritis
CUI: C0029408
Disease: Degenerative polyarthritis
247 0.716 0.480 X 49259429 intron variant T/C snv 0.010 1.000 1 2018 2018
Human papilloma virus infection
CUI: C0343641
Disease: Human papilloma virus infection
42 0.716 0.480 X 49259429 intron variant T/C snv 0.010 1.000 1 2019 2019
Kidney Failure, Chronic
CUI: C0022661
Disease: Kidney Failure, Chronic
425 0.716 0.480 X 49259429 intron variant T/C snv 0.010 1.000 1 2016 2016
Malignant neoplasm of breast
CUI: C0006142
Disease: Malignant neoplasm of breast
3417 0.716 0.480 X 49259429 intron variant T/C snv 0.010 1.000 1 2017 2017
Multiple Sclerosis
CUI: C0026769
Disease: Multiple Sclerosis
1022 0.716 0.480 X 49259429 intron variant T/C snv 0.010 1.000 1 2019 2019
Rheumatoid Arthritis
CUI: C0003873
Disease: Rheumatoid Arthritis
2387 0.716 0.480 X 49259429 intron variant T/C snv 0.010 1.000 1 2016 2016
Squamous intraepithelial lesion
CUI: C0333873
Disease: Squamous intraepithelial lesion
8 0.716 0.480 X 49259429 intron variant T/C snv 0.010 1.000 1 2019 2019
Ulcerative Colitis
CUI: C0009324
Disease: Ulcerative Colitis
827 0.716 0.480 X 49259429 intron variant T/C snv 0.010 1.000 1 2019 2019
Vitiligo
CUI: C0042900
Disease: Vitiligo
249 0.716 0.480 X 49259429 intron variant T/C snv 0.010 1.000 1 2013 2013
VITILIGO-ASSOCIATED MULTIPLE AUTOIMMUNE DISEASE SUSCEPTIBILITY 1 (finding)
CUI: C1847835
Disease: VITILIGO-ASSOCIATED MULTIPLE AUTOIMMUNE DISEASE SUSCEPTIBILITY 1 (finding)
92 0.716 0.480 X 49259429 intron variant T/C snv 0.010 1.000 1 2013 2013