KIF1A NM_001244008.2(KIF1A):c.3901+8C>A

CI-VAR-00332324Explore in graph →NM_001244008.2:c.3901+8C>AClinVar 2934087 rs1461765194

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
2934087	Likely benign	criteria provided, single submitter	1	Neuropathy, hereditary sensory, type 2C; Hereditary spastic paraplegia 30; Intellectual disability, autosomal dominant 9; Uterine corpus endometrial carcinoma	germline	2	Jan 26, 2023	clinvar