ClinVar Miner

List of variants in gene AMTN studied for amelogenesis imperfecta type 3B

Included ClinVar conditions (1):

Amelogenesis imperfecta type 3B

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 1

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HGVS	dbSNP	gnomAD frequency
NM_212557.4(AMTN):c.54+1348_330+98delinsCTCA

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