XYLT1 NM_022166.4(XYLT1):c.1588-3C>T

CI-VAR-00019424Explore in graph →NM_022166.4:c.1588-3C>TClinVar 127238 rs201818754

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
127238	Likely benign	criteria provided, multiple submitters, no conflicts	2	Desbuquois dysplasia 2; Desbuquois dysplasia 1; Autosomal recessive inherited pseudoxanthoma elasticum; XYLT1-related disorder; Colon adenocarcinoma; Ovarian serous cystadenocarcinoma; Gastric cancer; Malignant tumor of esophagus; Adrenocortical carcinoma, hereditary; Cervical cancer; Familial cancer of breast	germline	14	Apr 01, 2026	clinvar