rs77724903, RET

N. diseases: 23
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.
Pheochromocytoma
CUI: C0031511
Disease: Pheochromocytoma
186 0.672 0.280 10 43118460 missense variant A/G;T snv 4.0E-06; 2.1E-03 0.830 0.667 3 2010 2015
Familial medullary thyroid carcinoma
45 0.672 0.280 10 43118460 missense variant A/G;T snv 4.0E-06; 2.1E-03 0.810 1.000 21 1993 2007
Multiple Endocrine Neoplasia Type 2a
44 0.672 0.280 10 43118460 missense variant A/G;T snv 4.0E-06; 2.1E-03 0.810 0.929 14 1993 2013
Medullary carcinoma of thyroid
CUI: C0238462
Disease: Medullary carcinoma of thyroid
71 0.672 0.280 10 43118460 missense variant A/G;T snv 4.0E-06; 2.1E-03 0.750 0.833 6 2005 2015
Hirschsprung Disease
CUI: C0019569
Disease: Hirschsprung Disease
162 0.672 0.280 10 43118460 missense variant A/G;T snv 4.0E-06; 2.1E-03 0.720 1.000 2 2009 2013
HIRSCHSPRUNG DISEASE, SUSCEPTIBILITY TO, 1
52 0.672 0.280 10 43118460 missense variant A/G;T snv 4.0E-06; 2.1E-03 0.700 1.000 15 1994 2011
Multiple Endocrine Neoplasia Type 1
CUI: C0025267
Disease: Multiple Endocrine Neoplasia Type 1
156 0.672 0.280 10 43118460 missense variant A/G;T snv 4.0E-06; 2.1E-03 0.700 1.000 1 2005 2005
Multiple Endocrine Neoplasia Type 2b
21 0.672 0.280 10 43118460 missense variant A/G;T snv 4.0E-06; 2.1E-03 0.700 1.000 1 2005 2005
Multiple Endocrine Neoplasia, Type IV
23 0.672 0.280 10 43118460 missense variant A/G;T snv 4.0E-06; 2.1E-03 0.700 1.000 1 2005 2005
Breast Cancer, Familial
CUI: C0346153
Disease: Breast Cancer, Familial
91 0.672 0.280 10 43118460 missense variant A/G;T snv 4.0E-06; 2.1E-03 0.700 0
Malignant neoplasm of breast
CUI: C0006142
Disease: Malignant neoplasm of breast
3417 0.672 0.280 10 43118460 missense variant A/G;T snv 4.0E-06; 2.1E-03 0.700 0
Adrenal Gland Pheochromocytoma
CUI: C4551683
Disease: Adrenal Gland Pheochromocytoma
50 0.672 0.280 10 43118460 missense variant A/G;T snv 4.0E-06; 2.1E-03 0.030 0.667 3 2010 2015
Hyperparathyroidism, Primary
CUI: C0221002
Disease: Hyperparathyroidism, Primary
39 0.672 0.280 10 43118460 missense variant A/G;T snv 4.0E-06; 2.1E-03 0.020 1.000 2 2005 2005
Glioblastoma Multiforme
CUI: C1621958
Disease: Glioblastoma Multiforme
186 0.672 0.280 10 43118460 missense variant A/G;T snv 4.0E-06; 2.1E-03 0.010 1.000 1 2011 2011
Malignant neoplasm of stomach
CUI: C0024623
Disease: Malignant neoplasm of stomach
615 0.672 0.280 10 43118460 missense variant A/G;T snv 4.0E-06; 2.1E-03 0.010 1.000 1 2011 2011
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1641 0.672 0.280 10 43118460 missense variant A/G;T snv 4.0E-06; 2.1E-03 0.010 1 2013 2013
Multiple endocrine neoplasia Type 2
CUI: C4048306
Disease: Multiple endocrine neoplasia Type 2
38 0.672 0.280 10 43118460 missense variant A/G;T snv 4.0E-06; 2.1E-03 0.010 1 2013 2013
Paraganglioma
CUI: C0030421
Disease: Paraganglioma
36 0.672 0.280 10 43118460 missense variant A/G;T snv 4.0E-06; 2.1E-03 0.010 1.000 1 2005 2005
Pheochromocytoma, malignant
CUI: C0334419
Disease: Pheochromocytoma, malignant
1 0.672 0.280 10 43118460 missense variant A/G;T snv 4.0E-06; 2.1E-03 0.010 1.000 1 2009 2009
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
1374 0.672 0.280 10 43118460 missense variant A/G;T snv 4.0E-06; 2.1E-03 0.010 1 2013 2013
Stomach Carcinoma
CUI: C0699791
Disease: Stomach Carcinoma
652 0.672 0.280 10 43118460 missense variant A/G;T snv 4.0E-06; 2.1E-03 0.010 1.000 1 2011 2011
Thyroid carcinoma
CUI: C0549473
Disease: Thyroid carcinoma
145 0.672 0.280 10 43118460 missense variant A/G;T snv 4.0E-06; 2.1E-03 0.010 1.000 1 2007 2007
Von Hippel-Lindau Syndrome
CUI: C0019562
Disease: Von Hippel-Lindau Syndrome
187 0.672 0.280 10 43118460 missense variant A/G;T snv 4.0E-06; 2.1E-03 0.010 1.000 1 2010 2010