rs141185224, RET

N. diseases: 2
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Ovarian Failure, Premature
CUI: C0085215
Disease: Ovarian Failure, Premature
0.010 GeneticVariation BEFREE We report a new RET point mutation [R694Q (CGG-->CAG)], serendipitously found in a 23-yr-old woman with hypothyroidism due to atrophic Hashimoto's thyroiditis and primary ovarian failure, without altered calcitonin secretion. 15472167 2004
Hypothyroidism
CUI: C0020676
Disease: Hypothyroidism
0.010 GeneticVariation BEFREE We report a new RET point mutation [R694Q (CGG-->CAG)], serendipitously found in a 23-yr-old woman with hypothyroidism due to atrophic Hashimoto's thyroiditis and primary ovarian failure, without altered calcitonin secretion. 15472167 2004