ClinVar Miner

List of variants in gene KRT10 reported as uncertain significance by GeneDx

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: 2

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HGVS	dbSNP	gnomAD frequency
NM_000421.5(KRT10):c.1588T>C (p.Tyr530His)	rs756380270	0.00001
NM_000421.5(KRT10):c.1681_1683dup (p.Ser563dup)	rs1555548360

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