rs2439302, NRG1

N. diseases: 9
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 8 32574851 intron variant G/C snv 0.54 0.830 1.000 3 2012 2015
Papillary thyroid carcinoma
CUI: C0238463
Disease: Papillary thyroid carcinoma
204 0.776 0.200 8 32574851 intron variant G/C snv 0.54 0.050 1.000 5 2013 2018
Malignant neoplasm of thyroid
CUI: C0007115
Disease: Malignant neoplasm of thyroid
103 0.776 0.200 8 32574851 intron variant G/C snv 0.54 0.030 1.000 3 2012 2015
Thyroid Neoplasm
CUI: C0040136
Disease: Thyroid Neoplasm
135 0.776 0.200 8 32574851 intron variant G/C snv 0.54 0.030 1.000 3 2012 2015
Neoplasms
CUI: C0027651
Disease: Neoplasms
1644 0.776 0.200 8 32574851 intron variant G/C snv 0.54 0.020 1.000 2 2015 2016
Differentiated Thyroid Gland Carcinoma
CUI: C1337013
Disease: Differentiated Thyroid Gland Carcinoma
80 0.776 0.200 8 32574851 intron variant G/C snv 0.54 0.010 1 2016 2016
Hirschsprung Disease
CUI: C0019569
Disease: Hirschsprung Disease
162 0.776 0.200 8 32574851 intron variant G/C snv 0.54 0.010 1.000 1 2017 2017
Primary differentiated carcinoma of thyroid gland
CUI: C4722172
Disease: Primary differentiated carcinoma of thyroid gland
41 0.776 0.200 8 32574851 intron variant G/C snv 0.54 0.010 1 2016 2016
Secondary malignant neoplasm of lymph node
CUI: C0686619
Disease: Secondary malignant neoplasm of lymph node
188 0.776 0.200 8 32574851 intron variant G/C snv 0.54 0.010 1.000 1 2016 2016