TMEM216 NM_001173990.3(TMEM216):c.432-1G>C

CI-VAR-00019075Explore in graph →NM_001173990.3:c.432-1G>CClinVar 126297 rs10897158

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
126297	Benign	criteria provided, multiple submitters, no conflicts	2	Joubert syndrome; Meckel syndrome, type 2; Joubert syndrome 1; Joubert syndrome 2; Uterine corpus endometrial carcinoma	germline	15	Feb 04, 2026	clinvar