List of variants in gene COL7A1 reported as uncertain significance for Amelogenesis imperfecta type 1

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_000094.4(COL7A1):c.3605G>A (p.Arg1202His)	rs149011081	0.00166
NM_000094.4(COL7A1):c.2440+3A>C
NM_000094.4(COL7A1):c.3785T>C (p.Met1262Thr)

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