ABCC6 NM_001171.6(ABCC6):c.3507-3C>T

CI-VAR-00049624Explore in graph →NM_001171.6:c.3507-3C>TClinVar 281169 rs41278172

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
281169	Benign/Likely benign	criteria provided, multiple submitters, no conflicts	2	Autosomal recessive inherited pseudoxanthoma elasticum; Finnish congenital nephrotic syndrome; Pseudoxanthoma elasticum, forme fruste; Arterial calcification, generalized, of infancy, 2; Clear cell carcinoma of kidney; Sarcoma; Malignant tumor of esophagus; Lung cancer; Gastric cancer; Ovarian serous cystadenocarcinoma; Thymoma; Acute myeloid leukemia; Uterine corpus endometrial carcinoma; Colon adenocarcinoma; Nonpapillary renal cell carcinoma; Familial cancer of breast	germline	16	Jun 01, 2026	clinvar