List of variants in gene COL7A1 reported as uncertain significance by Institute for Clinical Genetics, University Hospital TU Dresden, University Hospital TU Dresden

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_000094.4(COL7A1):c.2045G>A (p.Arg682Gln)	rs772900092	0.00003
NM_000094.4(COL7A1):c.4445G>A (p.Arg1482Gln)	rs570707807	0.00003
NM_000094.4(COL7A1):c.3746T>C (p.Val1249Ala)	rs2045222215	0.00001
NM_000094.4(COL7A1):c.6573G>A (p.Pro2191=)	rs779416907

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