SLC26A5 NM_198999.3(SLC26A5):c.-53-2A>G

CI-VAR-00005467Explore in graph →NM_198999.3:c.-53-2A>GClinVar 5289 rs116900495

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
5289	Benign/Likely benign	criteria provided, multiple submitters, no conflicts	2	Autosomal recessive nonsyndromic hearing loss 61; Uterine corpus endometrial carcinoma; Lung cancer; Chronic lymphocytic leukemia/small lymphocytic lymphoma; Familial pancreatic carcinoma; Sarcoma; Thyroid cancer, nonmedullary, 1	germline	8	Sep 08, 2023	clinvar