Variants in gene KIT with conflicting interpretations "pathogenic" and "likely pathogenic"

Submission 1 (pathogenic) minimum review status:		Submission 1 (pathogenic) method:
Submission 2 (likely pathogenic) minimum review status:		Submission 2 (likely pathogenic) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 4

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HGVS	dbSNP	gnomAD frequency
NM_000222.3(KIT):c.1676T>A (p.Val559Asp)	rs121913517
NM_000222.3(KIT):c.1676T>C (p.Val559Ala)	rs121913517
NM_000222.3(KIT):c.1924A>G (p.Lys642Glu)	rs121913512
NM_000222.3(KIT):c.2466T>G (p.Asn822Lys)	rs121913514

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