[PMID 16118333] Polymorphisms in exon 13 and intron 14 of the RET protooncogene: genetic modifiers of medullary thyroid carcinoma?




[PMID 11302967] Analysis of the RET, GDNF, EDN3, and EDNRB genes in patients with intestinal neuronal dysplasia and Hirschsprung disease.

rs2472737

Parent Gene: RET

Importance: 1
Less common allele: A = 17%
More common allele: G = 83%
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