List of variants in gene COL17A1 reported as uncertain significance by Neuberg Centre For Genomic Medicine, NCGM

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_000494.4(COL17A1):c.1339G>T (p.Gly447Cys)	rs200223042
NM_000494.4(COL17A1):c.1445T>C (p.Leu482Pro)	rs2493344397
NM_000494.4(COL17A1):c.3523G>A (p.Gly1175Ser)

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