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

Submission 1 (benign) minimum review status:		Submission 1 (benign) method:
Submission 2 (likely benign) minimum review status:		Submission 2 (likely benign) 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: 16

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HGVS	dbSNP	gnomAD frequency
NM_000222.3(KIT):c.2586G>C (p.Leu862=)	rs3733542	0.16755
NM_000222.3(KIT):c.*217G>A	rs17084733	0.10193
NM_000222.3(KIT):c.1621A>C (p.Met541Leu)	rs3822214	0.07727
NM_000222.3(KIT):c.2394C>T (p.Ile798=)	rs55789615	0.02125
NM_000222.3(KIT):c.67+4G>A	rs72550820	0.00969
NM_000222.3(KIT):c.532G>A (p.Ala178Thr)	rs115585711	0.00342
NM_000222.3(KIT):c.1383A>G (p.Thr461=)	rs151016327	0.00324
NM_000222.3(KIT):c.2597-51T>C	rs368272654	0.00263
NM_000222.3(KIT):c.1120G>A (p.Val374Ile)	rs73137716	0.00218
NM_000222.3(KIT):c.1199A>G (p.Asn400Ser)	rs72549294	0.00215
NM_000222.3(KIT):c.2622G>A (p.Pro874=)	rs55817813	0.00188
NM_000222.3(KIT):c.2805T>A (p.Ile935=)	rs72549296	0.00176
NM_000222.3(KIT):c.200C>G (p.Thr67Ser)	rs144933028	0.00045
NM_000222.3(KIT):c.1694G>T (p.Gly565Val)	rs200945282	0.00009
NM_000222.3(KIT):c.1290A>G (p.Ala430=)	rs55966164	0.00004
NM_000222.3(KIT):c.252G>T (p.Thr84=)	rs56411694

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