List of variants in gene KRT16 reported as likely pathogenic by Fulgent Genetics, Fulgent Genetics

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_005557.4(KRT16):c.362T>C (p.Met121Thr)	rs28928894
NM_005557.4(KRT16):c.371T>A (p.Leu124His)	rs58293603
NM_005557.4(KRT16):c.375T>G (p.Asn125Lys)

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