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: rs11674595
rs11674595
IL1R2
0.763 0.200 2 101994530 intron variant T/C snv 0.22
CUI: C4048328
Disease: cervical cancer
cervical cancer 		0.010 1.000 1 2019 2019
dbSNP: rs11674595
rs11674595
IL1R2
0.763 0.200 2 101994530 intron variant T/C snv 0.22
CUI: C0546837
Disease: Malignant neoplasm of esophagus
Malignant neoplasm of esophagus 		0.010 1.000 1 2019 2019
dbSNP: rs11674595
rs11674595
IL1R2
0.763 0.200 2 101994530 intron variant T/C snv 0.22
CUI: C0549473
Disease: Thyroid carcinoma
Thyroid carcinoma 		0.010 1.000 1 2019 2019
dbSNP: rs11674595
rs11674595
IL1R2
0.763 0.200 2 101994530 intron variant T/C snv 0.22
CUI: C0041296
Disease: Tuberculosis
Tuberculosis 		0.010 1.000 1 2018 2018
dbSNP: rs11674595
rs11674595
IL1R2
0.763 0.200 2 101994530 intron variant T/C snv 0.22
CUI: C0030193
Disease: Pain
Pain 		0.010 1.000 1 2014 2014
dbSNP: rs11674595
rs11674595
IL1R2
0.763 0.200 2 101994530 intron variant T/C snv 0.22
CUI: C0007115
Disease: Malignant neoplasm of thyroid
Malignant neoplasm of thyroid 		0.010 1.000 1 2019 2019
dbSNP: rs11674595
rs11674595
IL1R2
0.763 0.200 2 101994530 intron variant T/C snv 0.22
CUI: C0024902
Disease: Mastodynia
Mastodynia 		0.010 1.000 1 2014 2014
dbSNP: rs11674595
rs11674595
IL1R2
0.763 0.200 2 101994530 intron variant T/C snv 0.22
CUI: C0014859
Disease: Esophageal Neoplasms
Esophageal Neoplasms 		0.010 1.000 1 2019 2019
dbSNP: rs11674595
rs11674595
IL1R2
0.763 0.200 2 101994530 intron variant T/C snv 0.22
CUI: C0302592
Disease: Cervix carcinoma
Cervix carcinoma 		0.010 1.000 1 2019 2019
dbSNP: rs11674595
rs11674595
IL1R2
0.763 0.200 2 101994530 intron variant T/C snv 0.22
CUI: C0152018
Disease: Esophageal carcinoma
Esophageal carcinoma 		0.010 1.000 1 2019 2019
dbSNP: rs11674595
rs11674595
IL1R2
0.763 0.200 2 101994530 intron variant T/C snv 0.22
CUI: C0007847
Disease: Malignant tumor of cervix
Malignant tumor of cervix 		0.010 1.000 1 2019 2019
dbSNP: rs11674595
rs11674595
IL1R2
0.763 0.200 2 101994530 intron variant T/C snv 0.22
CUI: C0040136
Disease: Thyroid Neoplasm
Thyroid Neoplasm 		0.010 1.000 1 2019 2019
dbSNP: rs11674595
rs11674595
IL1R2
0.763 0.200 2 101994530 intron variant T/C snv 0.22
CUI: C0553713
Disease: BREAST PAIN FEMALE
BREAST PAIN FEMALE 		0.010 1.000 1 2014 2014