rs76299620

This variant is located in the EFCAB13 gene.

ClinVar annotation

Benign
2 submitters

EFCAB13-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

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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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