RET NM_020975.6(RET):c.468C>T (p.Ala156=)

CI-VAR-00033848Explore in graph →p.Ala156=NM_020975.6:c.468C>TClinVar 215531 rs141290380

Curated evidence

Evidence by cancer (0 items)

Grouped by cancer context first, then therapy. The same variant can be sensitizing in one cancer and irrelevant in another — contexts are never merged. 50 items per page; a cancer group may continue on the next page.

Data not yet available

No curated evidence item references this variant yet.

ClinVar

Clinical significance (1)

ClinVar interpretations are shown as structured records — significance, review status, star rating, conditions — never flattened into one word.

clinvarCurated1 interpretation · review status and star rating as assigned by ClinVar.

Variation	Clinical significance	Review status	Stars	Conditions	Origin	Submitters	Last evaluated	Source
215531	Benign/Likely benign	criteria provided, multiple submitters, no conflicts	2	Multiple endocrine neoplasia, type 2; Hereditary cancer-predisposing syndrome; Familial medullary thyroid carcinoma; Pheochromocytoma; Multiple endocrine neoplasia type 2B; Hirschsprung disease, susceptibility to, 1; Multiple endocrine neoplasia type 2A	germline	9	Feb 02, 2026	clinvar