Variants in gene KIT with conflicting interpretations "uncertain significance" and "uncertain significance"

Submission 1 (uncertain significance) minimum review status:		Submission 1 (uncertain significance) method:
Submission 2 (uncertain significance) minimum review status:		Submission 2 (uncertain significance) 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.821C>T (p.Thr274Met)	rs138585275	0.00035
NM_000222.3(KIT):c.2263G>A (p.Ala755Thr)	rs201165084	0.00013
NM_000222.3(KIT):c.1694G>T (p.Gly565Val)	rs200945282	0.00009
NM_000222.3(KIT):c.839C>T (p.Ala280Val)	rs386833402	0.00004

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