rs965513, PTCSC2

N. diseases: 15
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.
Familial (FPAH)
CUI: C1611743
Disease: Familial (FPAH)
276 0.742 0.200 9 97793827 intron variant A/G;T snv 0.010 1.000 1 2012 2012
Nonmedullary Thyroid Carcinoma
CUI: C3501843
Disease: Nonmedullary Thyroid Carcinoma
3 0.742 0.200 9 97793827 intron variant A/G;T snv 0.010 1.000 1 2012 2012
Secondary Neoplasm
CUI: C2939419
Disease: Secondary Neoplasm
85 0.742 0.200 9 97793827 intron variant A/G;T snv 0.010 1.000 1 2014 2014
Secondary malignant neoplasm of lymph node
188 0.742 0.200 9 97793827 intron variant A/G;T snv 0.020 1.000 2 2014 2019
Neoplasm Metastasis
CUI: C0027627
Disease: Neoplasm Metastasis
327 0.742 0.200 9 97793827 intron variant A/G;T snv 0.030 1.000 3 2014 2019
Neoplasms
CUI: C0027651
Disease: Neoplasms
1644 0.742 0.200 9 97793827 intron variant A/G;T snv 0.040 1.000 4 2014 2019
Primary differentiated carcinoma of thyroid gland
41 0.742 0.200 9 97793827 intron variant A/G;T snv 0.050 0.600 5 2014 2016
Malignant neoplasm of thyroid
CUI: C0007115
Disease: Malignant neoplasm of thyroid
103 0.742 0.200 9 97793827 intron variant A/G;T snv 0.060 1.000 6 2012 2016
Thyroid Neoplasm
CUI: C0040136
Disease: Thyroid Neoplasm
135 0.742 0.200 9 97793827 intron variant A/G;T snv 0.060 1.000 6 2012 2016
Differentiated Thyroid Gland Carcinoma
80 0.742 0.200 9 97793827 intron variant A/G;T snv 0.070 0.714 7 2014 2018
Papillary thyroid carcinoma
CUI: C0238463
Disease: Papillary thyroid carcinoma
204 0.742 0.200 9 97793827 intron variant A/G;T snv 0.100 0.917 12 2011 2017
Hypothyroidism
CUI: C0020676
Disease: Hypothyroidism
283 0.742 0.200 9 97793827 intron variant A/G;T snv 0.700 1.000 2 2011 2012
Nasopharyngeal carcinoma
CUI: C2931822
Disease: Nasopharyngeal carcinoma
320 0.742 0.200 9 97793827 intron variant A/G;T snv 0.700 1.000 1 2010 2010
Polysomnography
CUI: C0162701
Disease: Polysomnography
249 0.742 0.200 9 97793827 intron variant A/G;T snv 0.700 1.000 1 2012 2012
Thyroid carcinoma
CUI: C0549473
Disease: Thyroid carcinoma
145 0.742 0.200 9 97793827 intron variant A/G;T snv 0.860 1.000 10 2009 2016