rs1867277, PTCSC2;FOXE1

N. diseases: 10
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.
Nonmedullary Thyroid Carcinoma
CUI: C3501843
Disease: Nonmedullary Thyroid Carcinoma
3 0.776 0.160 9 97853632 5 prime UTR variant A/G snv 0.63 0.010 1.000 1 2012 2012
Differentiated Thyroid Gland Carcinoma
80 0.776 0.160 9 97853632 5 prime UTR variant A/G snv 0.63 0.020 1.000 2 2015 2018
Malignant neoplasm of thyroid
CUI: C0007115
Disease: Malignant neoplasm of thyroid
103 0.776 0.160 9 97853632 5 prime UTR variant A/G snv 0.63 0.050 1.000 5 2009 2015
Thyroid Neoplasm
CUI: C0040136
Disease: Thyroid Neoplasm
135 0.776 0.160 9 97853632 5 prime UTR variant A/G snv 0.63 0.050 1.000 5 2009 2015
Thyroid carcinoma
CUI: C0549473
Disease: Thyroid carcinoma
145 0.776 0.160 9 97853632 5 prime UTR variant A/G snv 0.63 0.750 1.000 6 2009 2015
Tumor Cell Invasion
CUI: C1269955
Disease: Tumor Cell Invasion
169 0.776 0.160 9 97853632 5 prime UTR variant A/G snv 0.63 0.010 1.000 1 2015 2015
Papillary thyroid carcinoma
CUI: C0238463
Disease: Papillary thyroid carcinoma
204 0.776 0.160 9 97853632 5 prime UTR variant A/G snv 0.63 0.080 0.750 8 2011 2017
Familial (FPAH)
CUI: C1611743
Disease: Familial (FPAH)
276 0.776 0.160 9 97853632 5 prime UTR variant A/G snv 0.63 0.010 1.000 1 2012 2012
Graves Disease
CUI: C0018213
Disease: Graves Disease
352 0.776 0.160 9 97853632 5 prime UTR variant A/G snv 0.63 0.010 1.000 1 2011 2011
Neoplasms
CUI: C0027651
Disease: Neoplasms
1644 0.776 0.160 9 97853632 5 prime UTR variant A/G snv 0.63 0.010 1.000 1 2013 2013