List of variants in gene combination KRT81, KRT86 reported as likely benign 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_001320198.2(KRT86):c.684T>C (p.Asn228=)	rs200750977	0.03259
NM_001320198.2(KRT86):c.1102T>C (p.Leu368=)	rs11170087	0.01184
NM_001320198.2(KRT86):c.1053T>C (p.Ala351=)	rs28733260

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