List of variants in gene combination KRT3, LOC126861527 reported as pathogenic for Corneal dystrophy, Meesmann, 2

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_057088.3(KRT3):c.1525G>A (p.Glu509Lys)	rs57872071	0.00001
NM_057088.3(KRT3):c.1493A>T (p.Glu498Val)	rs267607431
NM_057088.3(KRT3):c.1508G>C (p.Arg503Pro)	rs60410063

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