SLC37A4 NM_001164277.2(SLC37A4):c.149-14A>G

CI-VAR-00022544Explore in graph →NM_001164277.2:c.149-14A>GClinVar 139186 rs79849261

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
139186	Benign/Likely benign	criteria provided, multiple submitters, no conflicts	2	Glycogen storage disease, type I; Glucose-6-phosphate transport defect; Phosphate transport defect; Congenital disorder of glycosylation, type IIw; Sarcoma; Gastric cancer; Ovarian serous cystadenocarcinoma; Acute myeloid leukemia; Malignant tumor of esophagus	germline	10	Feb 04, 2026	clinvar