ClinVar Miner

List of variants in gene FAM20A studied for amelogenesis imperfecta-gingival hyperplasia syndrome

Included ClinVar conditions (1):
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Gene type:
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Total variants: 4
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NM_017565.4(FAM20A):c.32_33CT[1] (p.Leu12fs) rs587776911
NM_017565.4(FAM20A):c.406C>T (p.Arg136Ter) rs144411158
NM_017565.4(FAM20A):c.590-2A>G rs587776914
NM_017565.4(FAM20A):c.612del (p.Leu205fs) rs587777531

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