RET, ret proto-oncogene, 5979

N. diseases: 10; N. variants: 57
Source: UNIPROT ×
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs75030001
rs75030001
Entrez Id: 5979
Gene Symbol: RET
RET
CUI: C1833921
Disease:
Familial medullary thyroid carcinoma 		0.830 GeneticVariation UNIPROT
dbSNP: rs77724903
rs77724903
Entrez Id: 5979
Gene Symbol: RET
RET
CUI: C0031511
Disease:
Pheochromocytoma 		0.830 GeneticVariation UNIPROT
dbSNP: rs77709286
rs77709286
Entrez Id: 5979
Gene Symbol: RET
RET
CUI: C0031511
Disease:
Pheochromocytoma 		0.800 GeneticVariation UNIPROT
dbSNP: rs74799832
rs74799832
Entrez Id: 5979
Gene Symbol: RET
RET
CUI: C1833921
Disease:
Familial medullary thyroid carcinoma 		0.770 GeneticVariation UNIPROT
dbSNP: rs75076352
rs75076352
Entrez Id: 5979
Gene Symbol: RET
RET
CUI: C1833921
Disease:
Familial medullary thyroid carcinoma 		0.740 GeneticVariation UNIPROT
dbSNP: rs77316810
rs77316810
Entrez Id: 5979
Gene Symbol: RET
RET
CUI: C1833921
Disease:
Familial medullary thyroid carcinoma 		0.730 GeneticVariation UNIPROT
dbSNP: rs377767405
rs377767405
Entrez Id: 5979
Gene Symbol: RET
RET
CUI: C0025268
Disease:
Multiple Endocrine Neoplasia Type 2a 		0.710 GeneticVariation UNIPROT
dbSNP: rs1060499894
rs1060499894
Entrez Id: 5979
Gene Symbol: RET
RET
CUI: C3888239
Disease:
HIRSCHSPRUNG DISEASE, SUSCEPTIBILITY TO, 1 		0.700 GeneticVariation UNIPROT
dbSNP: rs121913308
rs121913308
Entrez Id: 5979
Gene Symbol: RET
RET
CUI: C0549473
Disease:
Thyroid carcinoma 		0.700 GeneticVariation UNIPROT
dbSNP: rs1255575160
rs1255575160
Entrez Id: 5979
Gene Symbol: RET
RET
CUI: C3888239
Disease:
HIRSCHSPRUNG DISEASE, SUSCEPTIBILITY TO, 1 		0.700 GeneticVariation UNIPROT
dbSNP: rs1318733775
rs1318733775
Entrez Id: 5979
Gene Symbol: RET
RET
CUI: C3888239
Disease:
HIRSCHSPRUNG DISEASE, SUSCEPTIBILITY TO, 1 		0.700 GeneticVariation UNIPROT
dbSNP: rs1451004715
rs1451004715
Entrez Id: 5979
Gene Symbol: RET
RET
CUI: C3888239
Disease:
HIRSCHSPRUNG DISEASE, SUSCEPTIBILITY TO, 1 		0.700 GeneticVariation UNIPROT
dbSNP: rs1477699803
rs1477699803
Entrez Id: 5979
Gene Symbol: RET
RET
CUI: C3888239
Disease:
HIRSCHSPRUNG DISEASE, SUSCEPTIBILITY TO, 1 		0.700 GeneticVariation UNIPROT
dbSNP: rs149403911
rs149403911
Entrez Id: 5979
Gene Symbol: RET
RET
CUI: C1319315
Disease:
Adenocarcinoma of large intestine 		0.700 GeneticVariation UNIPROT
dbSNP: rs192489011
rs192489011
Entrez Id: 5979
Gene Symbol: RET
RET
CUI: C1275808
Disease:
Congenital central hypoventilation 		0.700 GeneticVariation UNIPROT
dbSNP: rs200127630
rs200127630
Entrez Id: 5979
Gene Symbol: RET
RET
CUI: C3888239
Disease:
HIRSCHSPRUNG DISEASE, SUSCEPTIBILITY TO, 1 		0.700 GeneticVariation UNIPROT
dbSNP: rs377767391
rs377767391
Entrez Id: 5979
Gene Symbol: RET
RET
CUI: C0025268
Disease:
Multiple Endocrine Neoplasia Type 2a 		0.700 GeneticVariation UNIPROT
dbSNP: rs377767391
rs377767391
Entrez Id: 5979
Gene Symbol: RET
RET
CUI: C1833921
Disease:
Familial medullary thyroid carcinoma 		0.700 GeneticVariation UNIPROT
dbSNP: rs377767396
rs377767396
Entrez Id: 5979
Gene Symbol: RET
RET
CUI: C3888239
Disease:
HIRSCHSPRUNG DISEASE, SUSCEPTIBILITY TO, 1 		0.700 GeneticVariation UNIPROT
dbSNP: rs377767397
rs377767397
Entrez Id: 5979
Gene Symbol: RET
RET
CUI: C0025268
Disease:
Multiple Endocrine Neoplasia Type 2a 		0.700 GeneticVariation UNIPROT
dbSNP: rs377767405
rs377767405
Entrez Id: 5979
Gene Symbol: RET
RET
CUI: C1833921
Disease:
Familial medullary thyroid carcinoma 		0.700 GeneticVariation UNIPROT
dbSNP: rs377767430
rs377767430
Entrez Id: 5979
Gene Symbol: RET
RET
CUI: C3888239
Disease:
HIRSCHSPRUNG DISEASE, SUSCEPTIBILITY TO, 1 		0.700 GeneticVariation UNIPROT
dbSNP: rs377767432
rs377767432
Entrez Id: 5979
Gene Symbol: RET
RET
CUI: C1833921
Disease:
Familial medullary thyroid carcinoma 		0.700 GeneticVariation UNIPROT
dbSNP: rs541929171
rs541929171
Entrez Id: 5979
Gene Symbol: RET
RET
CUI: C3888239
Disease:
HIRSCHSPRUNG DISEASE, SUSCEPTIBILITY TO, 1 		0.700 GeneticVariation UNIPROT
dbSNP: rs562449603
rs562449603
Entrez Id: 5979
Gene Symbol: RET
RET
CUI: C3888239
Disease:
HIRSCHSPRUNG DISEASE, SUSCEPTIBILITY TO, 1 		0.700 GeneticVariation UNIPROT