rs966423, DIRC3

N. diseases: 11
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.
Thyroid carcinoma
CUI: C0549473
Disease: Thyroid carcinoma
145 0.776 0.200 2 217445617 intron variant C/G;T snv 0.820 1.000 2 2012 2013
Papillary thyroid carcinoma
CUI: C0238463
Disease: Papillary thyroid carcinoma
204 0.776 0.200 2 217445617 intron variant C/G;T snv 0.030 0.667 3 2013 2019
Malignant neoplasm of thyroid
CUI: C0007115
Disease: Malignant neoplasm of thyroid
103 0.776 0.200 2 217445617 intron variant C/G;T snv 0.020 1.000 2 2012 2013
Secondary malignant neoplasm of lymph node
CUI: C0686619
Disease: Secondary malignant neoplasm of lymph node
188 0.776 0.200 2 217445617 intron variant C/G;T snv 0.020 1.000 2 2016 2019
Thyroid Neoplasm
CUI: C0040136
Disease: Thyroid Neoplasm
135 0.776 0.200 2 217445617 intron variant C/G;T snv 0.020 1.000 2 2012 2013
Differentiated Thyroid Gland Carcinoma
CUI: C1337013
Disease: Differentiated Thyroid Gland Carcinoma
80 0.776 0.200 2 217445617 intron variant C/G;T snv 0.010 1.000 1 2016 2016
Laryngeal Squamous Cell Carcinoma
CUI: C0280324
Disease: Laryngeal Squamous Cell Carcinoma
30 0.776 0.200 2 217445617 intron variant C/G;T snv 0.010 1.000 1 2016 2016
Neoplasm Metastasis
CUI: C0027627
Disease: Neoplasm Metastasis
327 0.776 0.200 2 217445617 intron variant C/G;T snv 0.010 1.000 1 2019 2019
Neoplasms
CUI: C0027651
Disease: Neoplasms
1644 0.776 0.200 2 217445617 intron variant C/G;T snv 0.010 1.000 1 2019 2019
Primary differentiated carcinoma of thyroid gland
CUI: C4722172
Disease: Primary differentiated carcinoma of thyroid gland
41 0.776 0.200 2 217445617 intron variant C/G;T snv 0.010 1.000 1 2016 2016
Tumor Cell Invasion
CUI: C1269955
Disease: Tumor Cell Invasion
169 0.776 0.200 2 217445617 intron variant C/G;T snv 0.010 1.000 1 2016 2016