rs16973042

This variant is located in the FAM20A gene.

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ClinVar annotation

Likely Benign★★★☆
3 submitters2 publications

not provided; Amelogenesis imperfecta type 1G; Ovarian serous cystadenocarcinoma; Malignant tumor of esophagus; Gastric cancer; Acute myeloid leukemia; Lung cancer; Uterine corpus endometrial carcinoma

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About FAM20A

This locus encodes a protein that is likely secreted and may function in hematopoiesis. A mutation at this locus has been associated with amelogenesis imperfecta and gingival hyperplasia syndrome. Alternatively spliced transcript variants have been identified. [provided by RefSeq, Aug 2011]

View all FAM20A variants →

Gene information from NCBI Gene. Variant classifications from ClinVar.

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