rs11674595, IL1R2

N. diseases: 13
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 PAIN FEMALE
CUI: C0553713
Disease: BREAST PAIN FEMALE
3 0.763 0.200 2 101994530 intron variant T/C snv 0.22 0.010 1.000 1 2014 2014
cervical cancer
CUI: C4048328
Disease: cervical cancer
268 0.763 0.200 2 101994530 intron variant T/C snv 0.22 0.010 1.000 1 2019 2019
Cervix carcinoma
CUI: C0302592
Disease: Cervix carcinoma
283 0.763 0.200 2 101994530 intron variant T/C snv 0.22 0.010 1.000 1 2019 2019
Esophageal carcinoma
CUI: C0152018
Disease: Esophageal carcinoma
272 0.763 0.200 2 101994530 intron variant T/C snv 0.22 0.010 1.000 1 2019 2019
Esophageal Neoplasms
CUI: C0014859
Disease: Esophageal Neoplasms
270 0.763 0.200 2 101994530 intron variant T/C snv 0.22 0.010 1.000 1 2019 2019
Malignant neoplasm of esophagus
CUI: C0546837
Disease: Malignant neoplasm of esophagus
214 0.763 0.200 2 101994530 intron variant T/C snv 0.22 0.010 1.000 1 2019 2019
Malignant neoplasm of thyroid
CUI: C0007115
Disease: Malignant neoplasm of thyroid
103 0.763 0.200 2 101994530 intron variant T/C snv 0.22 0.010 1.000 1 2019 2019
Malignant tumor of cervix
CUI: C0007847
Disease: Malignant tumor of cervix
245 0.763 0.200 2 101994530 intron variant T/C snv 0.22 0.010 1.000 1 2019 2019
Mastodynia
CUI: C0024902
Disease: Mastodynia
3 0.763 0.200 2 101994530 intron variant T/C snv 0.22 0.010 1.000 1 2014 2014
Pain
CUI: C0030193
Disease: Pain
196 0.763 0.200 2 101994530 intron variant T/C snv 0.22 0.010 1.000 1 2014 2014
Thyroid carcinoma
CUI: C0549473
Disease: Thyroid carcinoma
145 0.763 0.200 2 101994530 intron variant T/C snv 0.22 0.010 1.000 1 2019 2019
Thyroid Neoplasm
CUI: C0040136
Disease: Thyroid Neoplasm
135 0.763 0.200 2 101994530 intron variant T/C snv 0.22 0.010 1.000 1 2019 2019
Tuberculosis
CUI: C0041296
Disease: Tuberculosis
328 0.763 0.200 2 101994530 intron variant T/C snv 0.22 0.010 1.000 1 2018 2018