rs10961917

This variant is located in the TTC39B gene.

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ClinVar annotation

Likely Benign★☆☆☆
2 submitters

not provided; Lung cancer; Cervical cancer; Familial cancer of breast; Gastric cancer; Ovarian serous cystadenocarcinoma; Thymoma; Thyroid cancer, nonmedullary, 1; Colon adenocarcinoma; Sarcoma; Melanoma; Malignant tumor of esophagus; Clear cell carcinoma of kidney; Colorectal cancer; Hepatocellular carcinoma; Nonpapillary renal cell carcinoma

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About TTC39B

Predicted to be involved in several processes, including cholesterol homeostasis; negative regulation of cholesterol storage; and regulation of cholesterol efflux. [provided by Alliance of Genome Resources, Jul 2025]

View all TTC39B variants →

Gene information from NCBI Gene. Variant classifications from ClinVar.

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