List of variants in gene KRT6A reported as likely benign by CeGaT Center for Human Genetics Tuebingen

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_005554.4(KRT6A):c.951T>C (p.Ser317=)	rs432834	0.00016
NM_005554.4(KRT6A):c.1449A>G (p.Gln483=)	rs372218481	0.00011
NM_005554.4(KRT6A):c.1206C>T (p.Cys402=)
NM_005554.4(KRT6A):c.1221C>T (p.Ala407=)

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