RET, ret proto-oncogene, 5979

N. diseases: 607; N. variants: 162
Disease: THYROID CARCINOMA, SPORADIC MEDULLARY ×
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: rs74799832
rs74799832 		0.662 0.280 10 43121968 missense variant T/C snv 4.0E-06
CUI: C1833929
Disease: THYROID CARCINOMA, SPORADIC MEDULLARY
THYROID CARCINOMA, SPORADIC MEDULLARY 		0.700 0
dbSNP: rs1799939
rs1799939 		0.658 0.280 10 43114671 missense variant G/A;C;T snv 0.21
CUI: C1833929
Disease: THYROID CARCINOMA, SPORADIC MEDULLARY
THYROID CARCINOMA, SPORADIC MEDULLARY 		0.030 1.000 3 2004 2008
dbSNP: rs146838520
rs146838520 		0.851 0.120 10 43120129 missense variant C/T snv 4.0E-06 2.8E-05
CUI: C1833929
Disease: THYROID CARCINOMA, SPORADIC MEDULLARY
THYROID CARCINOMA, SPORADIC MEDULLARY 		0.010 1.000 1 2006 2006
dbSNP: rs75076352
rs75076352 		0.689 0.240 10 43114500 missense variant T/A;C;G snv 1.2E-05
CUI: C1833929
Disease: THYROID CARCINOMA, SPORADIC MEDULLARY
THYROID CARCINOMA, SPORADIC MEDULLARY 		0.010 1.000 1 2018 2018
dbSNP: rs75234356
rs75234356 		0.716 0.240 10 43120144 missense variant T/G snv 1.2E-05 7.0E-06
CUI: C1833929
Disease: THYROID CARCINOMA, SPORADIC MEDULLARY
THYROID CARCINOMA, SPORADIC MEDULLARY 		0.010 1.000 1 2012 2012
dbSNP: rs75873440
rs75873440 		0.763 0.200 10 43112173 missense variant G/A;T snv 4.4E-05
CUI: C1833929
Disease: THYROID CARCINOMA, SPORADIC MEDULLARY
THYROID CARCINOMA, SPORADIC MEDULLARY 		0.010 1.000 1 2012 2012