IFT172 NM_015662.3(IFT172):c.184-10A>T

CI-VAR-00190512Explore in graph →NM_015662.3:c.184-10A>TClinVar 1122628 rs546122503

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
1122628	Likely benign	criteria provided, multiple submitters, no conflicts	2	Retinitis pigmentosa 71; Short-rib thoracic dysplasia 10 with or without polydactyly; Bardet-Biedl syndrome 20; IFT172-related disorder; Ovarian serous cystadenocarcinoma	germline	5	Aug 07, 2025	clinvar