ClinVar Miner

List of variants studied for Amelogenesis imperfecta hypomaturation type 2A2 by Victorian Clinical Genetics Services, Murdoch Childrens Research Institute

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Total variants: 2
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HGVS dbSNP gnomAD frequency
NM_004771.4(MMP20):c.954-2A>T rs140213840 0.00224
NM_004771.4(MMP20):c.103A>C (p.Arg35=) rs61751462 0.00009

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