List of variants in gene KRT2 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_000423.3(KRT2):c.536G>A (p.Arg179His)	rs202243677	0.00012
NM_000423.3(KRT2):c.1066T>C (p.Tyr356His)	rs766282919	0.00001
NM_000423.3(KRT2):c.1325T>G (p.Leu442Trp)	rs2498600001
NM_000423.3(KRT2):c.1694C>T (p.Ser565Phe)	rs1365527480
NM_000423.3(KRT2):c.1813G>C (p.Gly605Arg)	rs1941143057
NM_000423.3(KRT2):c.1912T>C (p.Phe638Leu)	rs1398961883

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