ClinVar Miner

List of variants studied for amelogenesis imperfecta type 1G by Medical Molecular Genetics, National Research Centre

Included ClinVar conditions (1):
Minimum submission review status: Collection method:
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Total variants: 1
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HGVS dbSNP gnomAD frequency
NM_017565.4(FAM20A):c.1219+3_1219+6del rs2086254952

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