SGCD NM_000337.6(SGCD):c.*7596A>G

CI-VAR-00051164Explore in graph →NM_000337.6:c.*7596A>GClinVar 352444 rs80115276

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
352444	Benign/Likely benign	criteria provided, multiple submitters, no conflicts	2	Qualitative or quantitative defects of delta-sarcoglycan; Dilated cardiomyopathy 1L; Autosomal recessive limb-girdle muscular dystrophy type 2F; Ovarian serous cystadenocarcinoma	germline	5	Feb 08, 2023	clinvar