REEP1 NM_001371279.1(REEP1):c.105+26C>T

CI-VAR-00201133Explore in graph →NM_001371279.1:c.105+26C>TClinVar 1290967 rs1863058

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
1290967	Benign	criteria provided, multiple submitters, no conflicts	2	Neuronopathy, distal hereditary motor, type 5B; Hereditary spastic paraplegia 31; Familial cancer of breast; Hepatocellular carcinoma	germline	4	Nov 07, 2021	clinvar