SLC26A4 NM_000441.2(SLC26A4):c.-3-2A>G

CI-VAR-00008524Explore in graph →NM_000441.2:c.-3-2A>GClinVar 43486 rs397516411

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
43486	Pathogenic/Likely pathogenic	criteria provided, multiple submitters, no conflicts	2	Autosomal recessive nonsyndromic hearing loss 4; Pendred syndrome; Rare genetic deafness; SLC26A4-related disorder; Nonpapillary renal cell carcinoma; Monogenic hearing loss; Inborn genetic diseases	germline	21	Mar 18, 2026	clinvar