List of variants in gene KRT6A 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: 6

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HGVS	dbSNP	gnomAD frequency
NM_005554.4(KRT6A):c.332G>A (p.Gly111Asp)	rs681063	0.00088
NM_005554.4(KRT6A):c.1157G>A (p.Arg386His)	rs371739150	0.00013
NM_005554.4(KRT6A):c.46C>T (p.Arg16Trp)	rs767267061	0.00002
NM_005554.4(KRT6A):c.1316del (p.Gln439fs)	rs1469944063	0.00001
NM_005554.4(KRT6A):c.1680_1681delinsTT (p.Lys560_Ser561delinsAsnCys)
NM_005554.4(KRT6A):c.821T>G (p.Val274Gly)

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