List of variants in gene KIT reported as benign by PreventionGenetics, part of Exact Sciences

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: 13

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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.1621A>C (p.Met541Leu)	rs3822214	0.07727
NM_000222.3(KIT):c.2142-36A>G	rs17084713	0.02490
NM_000222.3(KIT):c.1638A>G (p.Lys546=)	rs55986963	0.02258
NM_000222.3(KIT):c.2394C>T (p.Ile798=)	rs55789615	0.02125
NM_000222.3(KIT):c.2847C>T (p.Pro949=)	rs56288823	0.01843
NM_000222.3(KIT):c.67+4G>A	rs72550820	0.00969
NM_000222.3(KIT):c.1119C>T (p.Tyr373=)	rs72549293	0.00964
NM_000222.3(KIT):c.532G>A (p.Ala178Thr)	rs115585711	0.00342
NM_000222.3(KIT):c.1199A>G (p.Asn400Ser)	rs72549294	0.00215
NM_000222.3(KIT):c.2805T>A (p.Ile935=)	rs72549296	0.00176
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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