List of variants in gene COL17A1 reported as uncertain significance for corneal disorder

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_000494.4(COL17A1):c.4081G>A (p.Gly1361Arg)	rs143021968	0.00023
NM_000494.4(COL17A1):c.2011G>A (p.Gly671Ser)
NM_000494.4(COL17A1):c.3071-5G>A	rs370589324
NM_000494.4(COL17A1):c.4142C>T (p.Ser1381Leu)	rs2086242885

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