SLC6A8 NM_005629.4(SLC6A8):c.1768-3C>T

CI-VAR-00033205Explore in graph →NM_005629.4:c.1768-3C>TClinVar 212213 rs150207268

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
212213	Benign/Likely benign	criteria provided, multiple submitters, no conflicts	2	Creatine transporter deficiency; Creatine deficiency syndrome 1; Inborn genetic diseases; SLC6A8-related disorder; Sarcoma; Ovarian serous cystadenocarcinoma; Cervical cancer; Familial cancer of breast; Uterine corpus endometrial carcinoma; Clear cell carcinoma of kidney; Ovarian cancer	germline	13	Feb 03, 2026	clinvar