LRRK2 NM_198578.4(LRRK2):c.6844-7G>T

CI-VAR-00132198Explore in graph →NM_198578.4:c.6844-7G>TClinVar 767036 rs200515208

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
767036	Likely benign	criteria provided, single submitter	1	Autosomal dominant Parkinson disease 8; Sarcoma; Ovarian serous cystadenocarcinoma; Acute myeloid leukemia; Lung cancer; Familial cancer of breast; Cervical cancer	germline	2	Apr 10, 2025	clinvar