RET, ret proto-oncogene, 5979

N. diseases: 607; N. variants: 162
Disease: Familial medullary thyroid carcinoma ×
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs377767398
rs377767398 		0.807 0.280 10 43113628 missense variant GC/AT;CT;TT mnv
CUI: C1833921
Disease: Familial medullary thyroid carcinoma
Familial medullary thyroid carcinoma 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Endocrine System Diseases 0.030 1.000 3 2001 2018
dbSNP: rs121913306
rs121913306 		0.851 0.120 10 43120119 missense variant AGC/TTT mnv
CUI: C1833921
Disease: Familial medullary thyroid carcinoma
Familial medullary thyroid carcinoma 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Endocrine System Diseases 0.020 1.000 2 1999 2017
dbSNP: rs377767429
rs377767429 		0.790 0.120 10 43120120 missense variant GC/TT mnv
CUI: C1833921
Disease: Familial medullary thyroid carcinoma
Familial medullary thyroid carcinoma 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Endocrine System Diseases 0.020 1.000 2 1999 2017
dbSNP: rs1206969193
rs1206969193 		0.925 0.200 10 43112117 missense variant G/A snv
CUI: C1833921
Disease: Familial medullary thyroid carcinoma
Familial medullary thyroid carcinoma 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Endocrine System Diseases 0.010 1.000 1 2015 2015
dbSNP: rs143795581
rs143795581 		0.851 0.120 10 43114596 missense variant A/C;G snv 8.0E-06
CUI: C1833921
Disease: Familial medullary thyroid carcinoma
Familial medullary thyroid carcinoma 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Endocrine System Diseases 0.010 1.000 1 2011 2011
dbSNP: rs1799939
rs1799939 		0.658 0.280 10 43114671 missense variant G/A;C;T snv 0.21
CUI: C1833921
Disease: Familial medullary thyroid carcinoma
Familial medullary thyroid carcinoma 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Endocrine System Diseases 0.010 1.000 1 2011 2011
dbSNP: rs377767395
rs377767395 		0.882 0.120 10 43113613 missense variant A/G snv
CUI: C1833921
Disease: Familial medullary thyroid carcinoma
Familial medullary thyroid carcinoma 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Endocrine System Diseases 0.010 1.000 1 2016 2016
dbSNP: rs377767404
rs377767404 		0.742 0.160 10 43114488 missense variant T/C snv
CUI: C1833921
Disease: Familial medullary thyroid carcinoma
Familial medullary thyroid carcinoma 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Endocrine System Diseases 0.010 1.000 1 2004 2004
dbSNP: rs377767415
rs377767415 		0.925 0.120 10 43118418 missense variant A/G snv 4.0E-06
CUI: C1833921
Disease: Familial medullary thyroid carcinoma
Familial medullary thyroid carcinoma 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Endocrine System Diseases 0.010 1.000 1 2006 2006
dbSNP: rs377767427
rs377767427 		0.882 0.120 10 43120114 missense variant C/G snv 4.0E-06
CUI: C1833921
Disease: Familial medullary thyroid carcinoma
Familial medullary thyroid carcinoma 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Endocrine System Diseases 0.010 1.000 1 2019 2019
dbSNP: rs377767442
rs377767442 		0.827 0.160 10 43121967 missense variant A/G snv
CUI: C1833921
Disease: Familial medullary thyroid carcinoma
Familial medullary thyroid carcinoma 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Endocrine System Diseases 0.010 1.000 1 2016 2016