rs3783521, IL1A

N. diseases: 8
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.
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
1962 0.807 0.200 2 112786000 upstream gene variant G/A snv 0.26 0.010 1.000 1 2019 2019
Conventional (Clear Cell) Renal Cell Carcinoma
CUI: C0279702
Disease: Conventional (Clear Cell) Renal Cell Carcinoma
222 0.807 0.200 2 112786000 upstream gene variant G/A snv 0.26 0.010 1.000 1 2017 2017
Malignant neoplasm of thyroid
CUI: C0007115
Disease: Malignant neoplasm of thyroid
103 0.807 0.200 2 112786000 upstream gene variant G/A snv 0.26 0.010 1.000 1 2019 2019
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1641 0.807 0.200 2 112786000 upstream gene variant G/A snv 0.26 0.010 1.000 1 2019 2019
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
1374 0.807 0.200 2 112786000 upstream gene variant G/A snv 0.26 0.010 1.000 1 2019 2019
Renal Cell Carcinoma
CUI: C0007134
Disease: Renal Cell Carcinoma
288 0.807 0.200 2 112786000 upstream gene variant G/A snv 0.26 0.010 1.000 1 2017 2017
Thyroid carcinoma
CUI: C0549473
Disease: Thyroid carcinoma
145 0.807 0.200 2 112786000 upstream gene variant G/A snv 0.26 0.010 1.000 1 2019 2019
Thyroid Neoplasm
CUI: C0040136
Disease: Thyroid Neoplasm
135 0.807 0.200 2 112786000 upstream gene variant G/A snv 0.26 0.010 1.000 1 2019 2019