rs75873440, RET

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.
Familial medullary thyroid carcinoma
CUI: C1833921
Disease: Familial medullary thyroid carcinoma
45 0.763 0.200 10 43112173 missense variant G/A;T snv 4.4E-05 0.730 1.000 3 2003 2008
Multiple endocrine neoplasia Type 2
CUI: C4048306
Disease: Multiple endocrine neoplasia Type 2
38 0.763 0.200 10 43112173 missense variant G/A;T snv 4.4E-05 0.710 1.000 10 2003 2014
Medullary carcinoma of thyroid
CUI: C0238462
Disease: Medullary carcinoma of thyroid
71 0.763 0.200 10 43112173 missense variant G/A;T snv 4.4E-05 0.070 1.000 7 2008 2017
Multiple Endocrine Neoplasia Type 2a
CUI: C0025268
Disease: Multiple Endocrine Neoplasia Type 2a
44 0.763 0.200 10 43112173 missense variant G/A;T snv 4.4E-05 0.040 1.000 4 2008 2014
Adrenal Gland Pheochromocytoma
CUI: C4551683
Disease: Adrenal Gland Pheochromocytoma
50 0.763 0.200 10 43112173 missense variant G/A;T snv 4.4E-05 0.020 1.000 2 2008 2011
Pheochromocytoma
CUI: C0031511
Disease: Pheochromocytoma
186 0.763 0.200 10 43112173 missense variant G/A;T snv 4.4E-05 0.020 1.000 2 2008 2011
Secondary malignant neoplasm of lymph node
CUI: C0686619
Disease: Secondary malignant neoplasm of lymph node
188 0.763 0.200 10 43112173 missense variant G/A;T snv 4.4E-05 0.020 1.000 2 2009 2014
Neoplasms, Second Primary
CUI: C0085183
Disease: Neoplasms, Second Primary
2 0.763 0.200 10 43112173 missense variant G/A;T snv 4.4E-05 0.010 1.000 1 2017 2017
Secondary malignant neoplasm of liver
CUI: C0494165
Disease: Secondary malignant neoplasm of liver
34 0.763 0.200 10 43112173 missense variant G/A;T snv 4.4E-05 0.010 1.000 1 2011 2011
THYROID CARCINOMA, SPORADIC MEDULLARY
CUI: C1833929
Disease: THYROID CARCINOMA, SPORADIC MEDULLARY
11 0.763 0.200 10 43112173 missense variant G/A;T snv 4.4E-05 0.010 1.000 1 2012 2012