List of variants in gene KRT10 reported as pathogenic for epidermolytic hyperkeratosis 2B, autosomal recessive

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_000421.5(KRT10):c.1281C>A (p.Cys427Ter)	rs387906640
NM_000421.5(KRT10):c.1300C>T (p.Gln434Ter)	rs60035576
NM_000421.5(KRT10):c.1314_1315insC (p.Lys439fs)	rs267607379

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