Source: ALL

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: rs2072472
rs2072472
IL1R2
0.732 0.200 2 102026557 intron variant A/G snv 0.24
CUI: C0152018
Disease: Esophageal carcinoma
Esophageal carcinoma 		0.010 1.000 1 2019 2019
dbSNP: rs2072472
rs2072472
IL1R2
0.732 0.200 2 102026557 intron variant A/G snv 0.24
CUI: C1306460
Disease: Primary malignant neoplasm of lung
Primary malignant neoplasm of lung 		0.010 1.000 1 2019 2019
dbSNP: rs2072472
rs2072472
IL1R2
0.732 0.200 2 102026557 intron variant A/G snv 0.24
CUI: C0546837
Disease: Malignant neoplasm of esophagus
Malignant neoplasm of esophagus 		0.010 1.000 1 2019 2019
dbSNP: rs2072472
rs2072472
IL1R2
0.732 0.200 2 102026557 intron variant A/G snv 0.24
CUI: C0242379
Disease: Malignant neoplasm of lung
Malignant neoplasm of lung 		0.010 1.000 1 2019 2019
dbSNP: rs2072472
rs2072472
IL1R2
0.732 0.200 2 102026557 intron variant A/G snv 0.24
CUI: C0684249
Disease: Carcinoma of lung
Carcinoma of lung 		0.010 1.000 1 2019 2019
dbSNP: rs2072472
rs2072472
IL1R2
0.732 0.200 2 102026557 intron variant A/G snv 0.24
CUI: C0040136
Disease: Thyroid Neoplasm
Thyroid Neoplasm 		0.010 1.000 1 2019 2019
dbSNP: rs2072472
rs2072472
IL1R2
0.732 0.200 2 102026557 intron variant A/G snv 0.24
CUI: C0340100
Disease: High altitude pulmonary edema
High altitude pulmonary edema 		0.010 1.000 1 2019 2019
dbSNP: rs2072472
rs2072472
IL1R2
0.732 0.200 2 102026557 intron variant A/G snv 0.24
CUI: C0007115
Disease: Malignant neoplasm of thyroid
Malignant neoplasm of thyroid 		0.010 1.000 1 2019 2019
dbSNP: rs2072472
rs2072472
IL1R2
0.732 0.200 2 102026557 intron variant A/G snv 0.24
CUI: C0476089
Disease: Endometrial Carcinoma
Endometrial Carcinoma 		0.010 1.000 1 2019 2019
dbSNP: rs2072472
rs2072472
IL1R2
0.732 0.200 2 102026557 intron variant A/G snv 0.24
CUI: C0549473
Disease: Thyroid carcinoma
Thyroid carcinoma 		0.010 1.000 1 2019 2019
dbSNP: rs2072472
rs2072472
IL1R2
0.732 0.200 2 102026557 intron variant A/G snv 0.24
CUI: C0014859
Disease: Esophageal Neoplasms
Esophageal Neoplasms 		0.010 1.000 1 2019 2019
dbSNP: rs2072472
rs2072472
IL1R2
0.732 0.200 2 102026557 intron variant A/G snv 0.24
CUI: C0007103
Disease: Malignant neoplasm of endometrium
Malignant neoplasm of endometrium 		0.010 1.000 1 2019 2019
dbSNP: rs2072472
rs2072472
IL1R2
0.732 0.200 2 102026557 intron variant A/G snv 0.24
CUI: C0014175
Disease: Endometriosis
Endometriosis 		0.010 1.000 1 2012 2012