rs76299620
This variant is located in the EFCAB13 gene.
▶ClinVar annotation
Benign
2 submittersEFCAB13-related disorder; Melanoma; Acute myeloid leukemia; Hepatocellular carcinoma; Nonpapillary renal cell carcinoma; Sarcoma; Thymoma; Cervical cancer; Uterine corpus endometrial carcinoma; Malignant lymphoma, large B-cell, diffuse; Colon adenocarcinoma; Ovarian serous cystadenocarcinoma; Thyroid cancer, nonmedullary, 1; Lung cancer
View on ClinVar →This variant is in our database but has no known associations or PRS memberships yet.
Gene information from NCBI Gene. Variant classifications from ClinVar.
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