List of variants in gene KRT10 reported as likely pathogenic for not provided

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.1345T>C (p.Tyr449His)	rs2143133897
NM_000421.5(KRT10):c.461A>G (p.Asn154Ser)	rs2143150923
NM_000421.5(KRT10):c.494G>C (p.Arg165Pro)	rs755924637

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