List of variants in gene KRT16 reported as benign for keratosis

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_005557.4(KRT16):c.1281-16T>C	rs7406899	0.96955
NM_005557.4(KRT16):c.624T>C (p.His208=)	rs4796681	0.65349

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