C19orf12 NM_001031726.4(C19orf12):c.164_166delGGG

CI-VAR-00015631Explore in graph →NM_001031726.4:c.164_166delGGGClinVar 88866 rs398122409

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
88866	Pathogenic/Likely pathogenic	criteria provided, multiple submitters, no conflicts	2	Neurodegeneration with brain iron accumulation 4; Neurodegeneration with brain iron accumulation; Hereditary spastic paraplegia 43; Neurofibromatosis, type 1; C19ORF12-related disorders	germline	11	Dec 30, 2025	clinvar