ClinVar Miner

List of variants studied for Amelogenesis imperfecta type 1F by OMIM

Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 2
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HGVS dbSNP gnomAD frequency
NM_016519.6(AMBN):c.294+140_531+479del
NM_016519.6(AMBN):c.532-1G>C rs146238585

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