List of variants in gene KRT14 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_000526.5(KRT14):c.856G>C (p.Glu286Gln)	rs202157466	0.00005
NM_000526.5(KRT14):c.1199T>G (p.Ile400Ser)	rs1352692209	0.00001
NM_000526.5(KRT14):c.1053+1G>A	rs1907411524
NM_000526.5(KRT14):c.1220G>A (p.Arg407Gln)	rs767154712
NM_000526.5(KRT14):c.851T>C (p.Leu284Pro)	rs2144583093
NM_000526.5(KRT14):c.856G>A (p.Glu286Lys)	rs202157466

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